Role of transcriptional networks in coordinating early events during kidney deve - 《American Journal of Physiology》美国生理学杂志干细胞之家



免疫细胞治疗专区	欢迎关注干细胞微信公众号

12 3 4 5 6 7 8 9 10 ... 25 下一页

返回列表

查看: 349064\|回复: 240	go Role of transcriptional networks in coordinating early events during kidney deve [复制链接]

轻羽

新手上路

Rank: 1

积分: 0
威望: 0
包包: 0

楼主

发表于 2009-4-22 08:41 |只看该作者 |倒序浏览 |打印

作者：Scott Boyle and Mark de Caestecker作者单位：Nephrology Division and Department of Cell and Developmental Biology, Vanderbilt University, Nashville, Tennessee


      , H/ h# \+ w7 x5 a/ {





                  ! n7 |/ O& H/ O2 s1 ^
      : U$ n, j; P+ p2 @7 H

      : o" m- y1 r! s/ H. d
      【摘要】
   Many of the signaling pathways that regulate tissue specification and coordinate cellular differentiation during embryogenesis have been identified over the last decade. These pathways are integrated at the transcriptional level, enabling activation of specific developmental programs in a temporally and spatially restricted fashion. Such developmental events are usually thought of in terms of hierarchical relationships, in which the expression of upstream factors leads to the sequential activation of a linear cascade of downstream genes. Whereas these models provide a simplistic approach to understand complex cellular events, genetic and biochemical studies in mice and other model organisms provide ample evidence that many of these factors interact at multiple levels in vivo and emphasize the importance of considering these linear events in context. The purpose of this review is to emphasize the complexity of these regulatory networks during the early phases of mammalian kidney development, outlining some of the limitations and alternative approaches that are being used to explore the complex nature of these networks in vivo. Before describing these networks in detail, we will provide a brief overview of the main structural changes and tissue interactions involved in mammalian kidney development, and go on to describe some of the limitations of our current approaches to evaluate the role of these developmental pathways in vivo. ; m: M+ c8 A  P( `7 B/ _
      【关键词】 transcription Drosophila eye development5 L2 W0 P8 u1 I. M8 X: T% t
   RENAL DEVELOPMENT IN MAMMALS/ Q1 N3 X; N2 z* M2 f6 x

THE KIDNEY HAS RECEIVED EXTENSIVE attention from developmental biologists since the nature of its reciprocal tissue interactions was first described more than 50 years ago ( 10, 38 ). There are three kidney structures that arise during mammalian development ( Fig. 1 A ). The pronephros and mesonephros develop first and are transient structures in mammals which serve as excretory organs during in utero development. Subsequently, the permanent kidney, or metanephros, is formed in the posterior aspect of the intermediate mesoderm, relying on similar tissue interactions involved in formation of the pro- and mesonephros ( 37 ). The first structural evidence of nephrogenesis arises around embryonic day 8 ( E8 ) in the mouse with the formation of two parallel epithelial tubes known as the nephric ducts within the intermediate mesoderm, in between the lateral and somitic mesoderm ( Fig. 1 B ). This occurs through mesenchyme-to-epithelial cell differentiation and is dependent on factors secreted by the overlying surface ectoderm and somites ( 23 ). Once formed, the nephric duct extends toward the posterior, or caudal, pole of the embryo, forming the core component of the developing urogenital system. The period between E8.5 and 9.5 is marked by formation of the pronephros and mesonephros, relying on many of the same genes required for metanephric development.
% X0 l8 T4 L: H4 k
Fig. 1. Early events in mammalian kidney development. A : sagittal view of kidney structures at embryonic day 10.5 ( E10.5 ). The pronephros forms at E8.5 along with the nephric duct, which emerges in the anterior intermediate mesoderm and elongates toward the cloaca. The mesonephros is present by E9.5 and serves as the excretory organ during in utero development. The metanephric mesenchyme (MM) first becomes visible at the level of the hindlimb at E10.5 adjacent to the posterior end of the nephric duct. B : cross section of an E8.0 embryo. Nephrogenic tissues are specified from the intermediate mesoderm by signals from the surface ectoderm and somites. C : ureteric bud outgrowth and early patterning of the MM. Gdnf expression by the MM induces outgrowth and invasion of the ureteric bud at E11. Ureteric bud invasion rescues the MM from apoptosis and stimulates the condensation of the cap mesenchyme around its tip.

The earliest changes associated with development of the metanephric kidney begin around E10.5 as cells within the posterior region of the intermediate mesoderm aggregate to form a population of cells known as the metanephric mesenchyme (MM). This group of cells contains precursors for epithelial, stromal, and vascular elements of the adult kidney. Formation of this structure is associated with the expression of a distinct profile of transcription factors within the posterior portion of the intermediate mesoderm ( Table 1 ). This culminates in the expression of the secreted growth factor Gdnf, which induces the outgrowth of the ureteric bud (UB) from the overlying nephric duct ( Fig. 1 C ) ( 27 ). All subsequent developmental events within the metanephric kidney are dependent on cellular interactions that are established as a result of the invasion of the UB into the MM. Initially, the UB secretes factors that rescue the MM from apoptosis and stimulate early patterning of the MM. This is associated with condensation of a subset of MM cells into a mesenchyme structure that aggregates tightly around the UB tip and is distinguishable from the surrounding loosely packed stromal mesenchyme ( Figs. 1 C and 2 A ). These events are dependent on outgrowth of the UB into the MM, but the specific signaling pathways and transcriptional programs that promote formation of the cap mesenchyme are unknown. Furthermore, it is uncertain whether establishment of the stromal compartment reflects migration of exogenous cells or expansion of precursor cells within the MM. The cap mesenchyme itself gives rise to most of the epithelial cells in the mature nephron, whereas the stromal compartment plays an important role in support and patterning of these differentiating cells.

Table 1. Transcription factors in the metanephric mesenchyme
( [* y* }' R% j7 O3 n* z, G0 M
Fig. 2. Formation and patterning of nephrons from the MM. A : early differentiation. The condensed cap mesenchyme becomes distinct from the surrounding stromal mesenchyme by E11.5. Early differentiation occurs at the ventral aspect with the appearance of the pretubular aggregate. By E12.5, the renal vesicle is evident as polarized columnar epithelial cells. B : nephron elongation, fusion with the ureteric bud, and vacularization. Nephrogenesis proceeds with the formation of the comma- and S-shaped bodies and early fusion of the future distal segment with ureteric bud epithelium. Endothelial cells invade the glomerular cleft of the S-shaped body. C : patterning of nephron segments. A second temporally distinct phase of nephrogenesis occurs after E16.5 in the mouse in which there is increased growth and patterning of nephron segments associated with expansion of the renal cortex and patterning of the medullary region of the adult kidney.1 [+ D! P$ ?  X& q! c( G9 R

Invasion of the UB initiates differentiation of the cap MM cells. This process is marked by the formation of small aggregates of cells contiguous with the ventral aspect of the cap structure called pretubular aggregates (PTA; Fig. 2 A ) ( 29 ). These cells undergo a burst of proliferation before they begin to express junctional and basement membrane markers, forming early polarized epithelial structures known as renal vesicles, first apparent at E12.5 in the mouse ( Fig. 2 A ) ( 2 ). Having established initial UB invasion, MM-derived signals provide for continued growth and symmetrical branching of the UB ( Fig. 1 C ). This, in turn, promotes patterning and differentiation of the newly forming cap mesenchyme within the outer, nephrogenic zone of the developing kidney. At the same time, PTA structures undergo further polarization as they form renal vesicles lined with columnar epithelium. These vesicles undergo a series of invaginations to form first comma- and then S-shaped-bodies, fusing with the extending UB to form a continuous lumen ( Fig. 2 B ). Distal elements elongate into the medulla, connecting the nephron to the UB-derived collecting system ( Fig. 2 C ). These events reflect initiation of a program of proximal and distal patterning that gives rise to distinct tubular segments and glomeruli and are associated with recruitment of stromal and vascular cell components of the developing kidney.$ N5 l5 S9 r% v% B

This process of UB branching and differentiation occurs throughout embryonic development, but 85% of the branching events that characterize mouse kidney development are complete by E16.5 ( 6 ). The iterative nature of these events suggests that there are likely to be populations of multipotent stem cells within the cap mesenchyme and UB bud tips that provide a continuous supply of epithelial progenitor cells as nephrogenesis progresses. These cells have yet to be positively identified. Detailed morphometric analysis indicates that there is a second, temporally distinct phase of nephrogenesis after E16.5 associated with a marked increase in tubular growth and patterning of nephron segments ( Fig. 2 C ) ( 6 ). This gives rise to expansion of the renal cortex and patterning of medullary regions of the adult kidney. Apart from glomerular podocytes ( 14 ), remarkably little is known about the signaling pathways and transcriptional programs regulating specification and patterning of the remaining nephron segments in the mammalian kidney.
8 \0 b2 D! f( t4 V' S; u$ j
TRANSCRIPTIONAL PROGRAMS INVOLVED IN EARLY METANEPHRIC KIDNEY DEVELOPMENT. U+ Q- O8 p6 s/ W5 Q" C5 |+ P$ {, p

Much of our understanding of the role of transcription factors in renal development stems from global deletion of individual genes expressed within the developing urogenital system. These studies have a number of intrinsic limitations. There is significant duplication of gene function in mammalian development, so that some of these mutations result in incomplete phenotypes that are difficult to interpret. A good example of this are mutations in the paralogous Hox11 gene cluster, where compound mutations of multiple components result in synergistic kidney phenotypes, whereas loss of individual genes has no effect on renal development ( 39 ). In addition, deletion of some genes, such as members of the cadherin family of junctional proteins ( 7 ), results in subtle defects that are only apparent through detailed analysis of nephron structure in adult mice. In practice, these studies are rarely performed if the mice are viable and have grossly normal kidneys. These issues are further complicated by the fact that genetic background can influence the phenotypic consequences of gene deletion. For example, deletion of Wnt4 on a pure genetic background demonstrated its requirement for all epithelial differentiation of the MM ( 33 ), whereas analysis of this mutation on a mixed background revealed that while kidneys were hypoplastic, they did contain differentiated nephrons ( 12 ). Furthermore, the interpretation of observed renal phenotypes relies to a large extent on the analysis of downstream gene expression by in situ hybridization. This is problematic, as the analysis of several mutant mice has demonstrated the importance of gene dosage in regulating these developmental events, a parameter that cannot be readily evaluated quantitatively using in situ hybridization techniques. Finally, failure to detect the expression of a putative downstream gene in a given mouse mutant does not necessarily indicate that it is directly regulated by the targeted gene, as the mutation may influence the survival and/or patterning of cell populations that normally express the gene of interest. This is further complicated by the fact that many of these developmental events are dependent on tissue interactions which are disorganized in mutant embryos. This has been a particular problem in analysis of genes involved in regulating the early events in kidney development.

Subject to these limitations, this review will discuss the major transcriptional programs that have been shown to play a clear role in regulating three phases of renal development: the regulation of nephric duct formation, the formation of the MM and regulation of UB outgrowth, and the regulation of early epithelial differentiation of the MM. We will outline some of the difficulties in interpreting mouse genetic models that have been used to establish the functional role of these programs in nephrogenesis and describe some of the new approaches that are being used to address outstanding questions. The reader is referred to Table 1 for a more comprehensive list of transcription factors and their proposed function in the MM and to a number of recent reviews and papers describing subsequent specification and patterning of nephron segments ( 3, 14, 43 ), stroma ( 3, 17, 18, 43 ), and the regulation of UB branching ( 3, 25 ).; I$ L4 K- u4 G6 E( B8 Q

Regulation of Nephric Duct Formation by Lim1, Pax2, and Pax8+ c8 _# x2 W: w7 i( M
- ^7 p! x0 G) `7 x( c* a6 |
Lim1, also known as Lhx1, is a homeodomain DNA-binding transcription factor that is initially detected in the visceral endoderm during gastrulation and is differentially expressed in multiple tissues during organ development ( 11, 13 ). In the developing urogenital system, expression is initiated in the lateral plate and intermediate mesoderm at E8.5. As the pro- and mesonephros are formed within the intermediate mesoderm, expression is lost in the lateral plate and becomes restricted to the mesonephric tubules and the nephric duct. Pax2 and Pax8 are two closely related members of a family of paired-box DNA-binding transcription factors that have largely overlapping expression domains in the developing kidney ( 4 ). Much like Lim1, Pax2 is expressed early in the intermediate mesoderm that gives rise to the renal anlage, and both Pax2 and Pax8 are expressed in the nephric duct as it extends posteriorly toward the cloaca ( 4, 9 ).

Global deletion of Lim1 is usually embryonically lethal due to a defect in formation of the placenta ( 32 ). The few mice that do survive until birth lack all intermediate mesoderm-derived structures, including the kidneys ( 36 ). More detailed analysis of these mutant mice indicates that Pax2 was initially expressed at low levels in the anterior portion of the intermediate mesoderm but failed to extend posteriorly into the nephrogenic region. Analysis of Hoxb6, which is normally expressed in the intermediate mesoderm and nephric duct, reveals markedly reduced expression in the Lim1 mutant mice in the region where the nephric duct, pro-, and mesonephric structures form. Expression of Hoxb6 is preserved, however, in the lateral plate. Taken together, these data suggest that Lim1 is specifically required for the differentiation of early nephrogenic structures within the intermediate mesoderm.' f% b# r( L( z

Like Lim1 mutants, deletion of Pax2 results in loss of the mesonephric tubules and the metanephric kidney ( 4, 34 ). In fact, marked kidney defects are observed in Pax2 heterozygotes, indicating that gene dosage is an important component of its function ( 34 ). Unlike the Lim1 mutants, however, the nephric duct forms in Pax2 mutants but fails to extend caudally to the level of metanephric development ( 34 ). Based on its wider expression in the intermediate mesoderm, it is surprising that the nephric duct forms at all in the absence of Pax2. The fact that Pax8 is also expressed in the nephric duct raises the possibility that it can functionally compensate for loss of Pax2 in this structure. Consistent with this, deletion of both Pax2 and Pax8 results in a complete failure of nephric duct formation ( 4 ). Interestingly, deletion of Pax8 alone does not disrupt formation of the meso- or metanephric kidney ( 20 ), suggesting that its function may be completely compensated for by Pax2 in the anterior intermediate mesoderm. The relationship between Lim1 and the Pax gene products during these early stages of kidney development is less clear. Most likely, the absence of Pax2 in the posterior intermediate mesoderm of Lim1 mutants reflects the failure of these differentiated structures to form and not direct regulation of Pax2 expression by Lim1 ( 36 ). However, our understanding of these early events in kidney development is limited to these descriptive studies, so that the precise relationship between these genes remains unclear.
0 O  M" c0 |, _
Specification of the MM and Regulation of UB Outgrowth by Eya1, Pax2, and Six1

Aside from formation and extension of the nephric duct, the establishment of the interactions between the MM and the UB is initially dependent on specification of the MM from the intermediate mesoderm and, subsequently, on the stimulation of UB outgrowth by the established MM. Eya1, Pax2, and Six1 are part of an evolutionarily conserved network of transcriptional regulators that have been shown to play a critical role in regulating both of these events. Important insights into the functional and biochemical relationships between components of this network have been elucidated from studies of their ancestral orthologs in the fruit fly ( 35 ). These studies provide an example of how our concepts of transcriptional control in vivo have shifted from linear to more complex networks and provide the basis to interpret results from the less malleable genetic models in mice. We will therefore spend some time summarizing results from genetic studies of this network in Drosophila before discussing the functional role of the orthologous system in during nephrogenesis.
0 |1 W1 J+ K. z. S) l" w/ g" l
Transcriptional networks in Drosophila eye development. Specification of cells that give rise to the eye in Drosophila is dependent on a network of transcriptionally active proteins within the eye-antennal imaginal disc, deletion of any of which results in loss of the eye (reviewed in Ref. 31 ). These are ancestral orthologs of the mammalian Eya, Pax, and Six family proteins that are also involved in development of the mammalian eye and include 1 ) eyes absent (eya), the fly ortholog of mammalian Eya family proteins (Eya1-4); this is a non-DNA-binding transcriptional cofactor that contains an NH 2 -terminal transactivation domain and requires the activity of other factors to activate or repress transcriptional responses; 2 ) sine oculis ( so ), a DNA-binding, homeodomain containing transcription factor related to mammalian Six proteins (Six1-6); 3 ) eyeless ( ey ), twin of eyeless ( toy ), and eyes gone ( eyg ) encode DNA-binding Pax-like proteins, containing the signature paired box domains; and 4 ) dachshund ( dac ), a non-DNA-binding cofactor related to the mammalian Dach proteins (Dach1/2).3 E6 Y3 \" T# j. K+ {
3 D0 n. K  a4 g3 a& }1 Z# W" M* P
Initial loss-of-function studies placed these proteins in a hierarchical arrangement initiated by toy, which goes on to activate a linear cascade of genes involved in eye development ( Fig. 3 A ). In reality, coordination of components within this pathway is more complex. Evidence for this comes from studies in which these genes have been misexpressed in tissues that do not normally form eyes. For example, misexpression of eya or dac, which are thought to act downstream of toy in this linear model, leads to the induction of toy expression and the formation of ectopic eyes. Furthermore, ectopic eye formation is more robust when combinations of ey, dac, and so are misexpressed. These findings indicate that more complex interactions exist between components of this transcriptional network than originally predicted ( Fig. 3 A ). Biochemical studies in mammalian cells support these observations and suggest potential mechanisms for some of these more complex circuits. For example, there is evidence that Six family proteins themselves interact with Eya1-3 in the cytoplasm and promote nuclear translocation of Eya-containing protein complexes ( 24 ). Furthermore, Dach1, the mammalian ortholog of dac, has been shown to repress Six1-dependent transcriptional responses, whereas Eya3 derepresses Dach1 by recruiting coactivators to the Six1/Dach1/DNA complexes ( Fig. 3 B ) ( 19 ). These findings provide a theoretical framework from which to interpret genetic studies of conserved programs involved in the early phases of nephrogenesis.: a( o( A- D5 o5 M$ j+ H
* }" w2 p6 ~6 Q8 ~
Fig. 3. Pax/ Eya /Six network. A : nonlinear transcriptional network during Drosophila eye development. Forward and reverse genetic interactions characterize this conserved network. toy, Twin of eyeless; ey, eyeless; eya, eyes absent; so, sine oculis; dac, dachshund. Mammalian orthologs are in parentheses. B : biochemical model of transcriptional control by Eya, Six, and Dach in mammalian cells. Dach1 acts as a repressor of Six1-dependent transcription. Eya3 derepresses this complex through recruitment of transcriptional activators.
8 F  z/ E, t* X/ Q5 [
Specification of the MM. Although the precise architecture of transcriptional networks in the MM is poorly understood, it is clear that Eya1 plays an essential role in regulating early events ( 28, 40, 42 ). Eya1 is one of four mammalian orthologs of Drosophila eyes absent ( eya ) and is expressed in the intermediate mesoderm from E8.5 and, more specifically, in the nephric duct and the uninduced MM at E10.5. As in the Drosophila eye, the expression domain of Eya1 in the MM overlaps with that of other members of the Eya/Six/Pax network. Mammalian so orthologs Six1 and Six2 are expressed in the MM before UB invasion, as are the toy and ey orthologs Pax2 and Pax8 ( 4, 41 ). The dac ortholog, Dach1, is expressed in early nephronic epithelia of the developing kidney ( 1 ); however, there are no published data relating to its functional role in renal development. Initial studies indicated that Eya1 null mutant mice died at birth with renal agenesis ( 40, 42 ). More detailed analysis has demonstrated that these mice form normal nephric duct and mesonephric tissues but fail to form the distinct MM aggregate at E10.5 in the posterior region of the intermediate mesoderm ( 28 ). To date, this is the only mutant identified that results in the failure of the MM to be specified from the intermediate mesoderm. As outlined above, Eya1 is a non-DNA-binding transcriptional cofactor that must interact with other DNA-binding factors to activate or repress transcription. This suggests that Eya1 expression alone is unlikely to be sufficient to specify the MM. Given the biochemical data demonstrating functional and physical interactions between Eya and Six family proteins ( 19, 24 ), it is possible that Eya1 acts by modifying the transcriptional activity of Six family members in the MM. Indeed, Six1 is coexpressed with Eya1 in the MM and Six1 null mice also fail to form kidneys ( 41 ), suggesting that specification may require the assembly of Six1/Eya1 complexes in the MM./ M$ N$ `$ I" o1 i

Stimulation of UB outgrowth from the nephric duct. In many of the mouse mutants that lack kidneys, the UB fails to emerge from the nephric duct, usually due to the failure of the uninduced MM to express Gdnf ( Table 1 ). Because of this, establishing the transcriptional network upstream of Gdnf has received considerable attention from the field in recent years. In vivo and in vitro studies clearly demonstrate a role for Pax2 in the regulation of Gdnf expression in the MM ( 5 ). In addition to the nephric duct, Pax2 is expressed in the MM before UB invasion ( 9 ), and the MM forms properly in Pax2 null mice but fails to express Gdnf ( 5 ). Pax2 binds and activates defined elements within the Gdnf promoter, suggesting that it may directly regulate Gdnf expression ( 5 ), but other components of this network up- and downstream of Pax2 are less clear. Based on their overlapping expression patterns and common phenotype, speculation has focused on other members of the Eya/Pax/Six network., O  G4 u  G7 J8 {: L

Initial characterization of the Eya1 knockout mouse at E11.5 revealed that expression of Pax2, Six1, and Gdnf were lost in the area of the MM ( 42 ), and previous studies have shown that Eya1 expression is independent of Pax2 ( 41 ). Together, these data make it tempting to speculate that Eya1 acts upstream of Pax2 and Six1 in a transcriptional circuit driving Gdnf expression in the MM. However, as discussed above, the MM never forms in Eya1 null mice, making it unclear whether these effects are due to the direct regulation of this pathway by Eya1 or simply a consequence of losing the MM. Furthermore, Gdnf expression is maintained in the MM of Six1 null mice despite the failure of the UB to emerge from the nephric duct ( 41 ). It is unclear whether this is simply an effect of reduced Gdnf dosage that is not demonstrated by in situ analysis of mRNA expression or if another, parallel pathway is required for UB outgrowth. For example, deletion of the Hoxa11/Hoxc11/Hoxd11 gene cluster also results in loss of Gdnf expression in the MM and the subsequent failure of UB outgrowth, despite normal expression of Pax2 ( 39 ). It is unclear whether these genes regulate Gdnf expression through an independent, nonredundant pathway or if they are part of a common transcriptional network downstream of Pax2. Once again, studies in the developing Drosophila eye may provide insight into these mechanisms. Overexpression of the Hox ortholog antennapedia in the eye inhibits transcriptional responses mediated by the Pax ortholog eyeless by competitive inhibition of DNA binding ( 26 ). If a similar mechanism is operative in the mammalian kidney, these findings would suggest that the Hox11 paralogs could play a direct role in modifying the transcriptional activity of Pax2. This would account for the loss of Gdnf expression while Pax2 expression is maintained in the Hoxa11/Hoxc11/Hoxd11 compound mutant mouse.

Early Epithelial Differentiation of the MM

The formation of early epithelial structures from the MM involves a host of coordinated cellular events that not only give rise to primitive nephrons but also replenish the MM for future rounds of differentiation. In vivo genetic studies of these events have been limited, as many of the factors that are expressed in the MM are also required for early specification and/or inductive events. Historically, this problem has been addressed in vitro by studying the ability of isolated MM structures from E11.5 mutant mouse embryos to undergo differentiation when exposed to potent inductive signals from spinal cord or wild-type UB isolates. This approach has enabled us to identify several so called "competence" factors that are required for this process ( Table 1 ), but it is unclear from these studies whether the apparent requirement for these factors in vitro actually reflects their functional role in the context of intact metanephroi. A good example of this problem comes from the analysis of Wt1 null mutant mice, in which there is complete loss of MM structures by E12.5 with no evidence of MM differentiation ( 15 ). Tissue recombination experiments demonstrated that wild-type spinal cord and UB structures are unable to rescue the Wt1 null MM phenotype in vitro ( 8, 15 ), suggesting that Wt1 could be a competence factor for MM differentiation. Loss of Wt1 is also associated with a marked increase in apoptosis of the uninduced MM over the 24-h period following its formation ( 15 ). The inappropriate death of MM cells in Wt1 null mice makes it impossible for tissue recombination experiments to determine whether the primary function of Wt1 is to act as a survival factor or whether it has an additional role in regulating MM differentiation.6 S& P, H2 t( e! V8 ?
  \0 o6 E/ i8 m/ l, T* \/ y
Many of these issues can now be circumvented using Cre/LoxP technology to delete genes in a spatially and temporally controlled manner. A recent example of this approach in the developing kidney is the deletion of Lim1 exclusively in MM-derived structures, bypassing its requirement for the formation of early nephrogenic structures, using Rarb2Cre and Lim1 LoxP mutant mice ( 12 ). These studies demonstrated that in the absence of Lim1, the PTA and renal vesicles form normally but fail to differentiate further or express nephron segment-specific markers, Dll1 or Brn1. These findings indicate that Lim1 is not required for initial differentiation of PTAs but is essential for subsequent patterning of the renal vesicle into tubular structures of the nephron. An alternative approach to study the function of genes that are essential for early patterning is to study in vivo cellular function in mosaic mice generated by introducing mutant ES cells along with lineage-specific markers into wild-type blastocysts. This approach has recently been used to evaluate the functional role of Ret signaling in regulating UB branching morphogenesis ( 31 ). By limiting the dosage of mutant cells, it was possible to track and study mutant cell function while preserving early renal development programs. Together, these conditional deletion and mosaic studies should enable us to determine the functional relationship between other MM-specific transcription factors, including Wt1 and Pax2, in coordination of differentiation events.6 K+ n+ Y- d& S: e' n! {( x: w* d
% C7 k% K2 M( s/ W
CONCLUSION/ h& V; Z8 b. W  c1 U& Y2 I
, Y/ a  J4 Y: B; c/ e
Genetic studies have demonstrated that transcription factors regulate critical events in metanephric development including establishing the nephrogenic field, specifying cell fate, and regulating differentiation of nephron precursors. It is apparent that these factors are integrated into evolutionarily conserved networks that cooperate to direct developmental events. While the power of mouse genetics has uncovered many individual factors in recent years, one of the major challenges that lies ahead is to understand how these genes cooperate in context to form networks accessible at multiple levels. Studies using mosaic and conditional mutant mice will allow us to address some of these issues. However, advances in understanding the complexity of the transcriptional networks involved in coordinating these events will only occur as findings from these studies in mice are fully integrated with genetic and biochemical data from other model systems.1 P& A& r* ^0 \, I4 X  `, S; N  \
      【参考文献】
Ayres JA, Shum L, Akarsu AN, Dashner R, Takahashi K, Ikura T, Slavkin HC, and Nuckolls GH. DACH: genomic characterization, evaluation as a candidate for postaxial polydactyly type A2, and developmental expression pattern of the mouse homologue. Genomics 77: 18-26, 2001.! t1 e0 O6 ]$ B# {) O9 ^! I

9 Z. E( I9 m  _/ L

Bard JB, Gordon A, Sharp L, and Sellers WI. Early nephron formation in the developing mouse kidney. J Anat 199: 385-392, 2001.
5 @# l( w: B* p& e' W+ q0 q
6 p/ f. {* [  [5 V% Y6 e- h( c

Bouchard M. Transcriptional control of kidney development. Differentiation 72: 295-306, 2004.

1 U1 u7 ]8 {" A8 R
Bouchard M, Souabni A, Mandler M, Neubuser A, and Busslinger M. Nephric lineage specification by Pax2 and Pax8. Genes Dev 16: 2958-2970, 2002.! v& Q6 M! O0 \) ]5 d
9 c8 B! \% ^6 r. T1 M2 g" R# A

2 L+ H) {+ u% g- c0 e) {6 i
Brophy PD, Ostrom L, Lang KM, and Dressler GR. Regulation of ureteric bud outgrowth by Pax2-dependent activation of the glial derived neurotrophic factor gene. Development 128: 4747-4756, 2001.

3 R, y  P0 N2 b& @2 h
' U+ q% B  L3 p
Cebrian C, Borodo K, Charles N, and Herzlinger DA. Morphometric index of the developing murine kidney. Dev Dyn 231: 601-608, 2004.2 U1 l1 ?) E. I+ S

Dahl U, Sjodin A, Larue L, Radice GL, Cajander S, Takeichi M, Kemler R, and Semb H. Genetic dissection of cadherin function during nephrogenesis. Mol Cell Biol 22: 1474-1487, 2002.
( g0 o! ?9 d8 i+ }
2 H' y: }8 ]7 E; `# T8 x8 T5 G& O
& w" ]. k, M& L  L2 g  y. T
Donovan MJ, Natoli TA, Sainio K, Amstutz A, Jaenisch R, Sariola H, and Kreidberg JA. Initial differentiation of the metanephric mesenchyme is independent of WT1 and the ureteric bud. Dev Genet 24: 252-262, 1999. <a href="/cgi/external_ref?access_num=10.1002/(SICI)1520-6408(1999)24:3/4
) x5 J5 h# T0 \/ e1 \4 A$ ^

  H$ E- k9 R6 n9 M% ~$ o
Dressler GR, Deutsch U, Chowdhury K, Nornes HO, and Gruss P. Pax2, a new murine paired-box-containing gene and its expression in the developing excretory system. Development 109: 787-795, 1990.4 m! n; u# g$ }2 D- H) s, I; `1 k
6 t& s. ]& M9 X: j# i8 g8 u

9 b, h$ f9 q3 ?  U. `9 d
Grobstein C. Inductive epitheliomesenchymal interaction in cultured organ rudiments of the mouse. Science 118: 52-55, 1953.( v  }3 L; j3 I. ]% s* P
6 Y! ]% r: `( Z, Y% B
: I2 e3 I7 _: n4 C2 R

Karavanov AA, Karavanova I, Perantoni A, and Dawid IB. Expression pattern of the rat Lim-1 homeobox gene suggests a dual role during kidney development. Int J Dev Biol 42: 61-66, 1998.( O2 x" s$ \8 S1 P; B
+ Y9 O4 P, I. k- n- k: [
6 }0 \2 ^# r$ u2 I% s% V- X

Kobayashi A, Kwan KM, Carroll TJ, McMahon AP, Mendelsohn CL, and Behringer RR. Distinct and sequential tissue-specific activities of the LIM-class homeobox gene Lim1 for tubular morphogenesis during kidney development. Development 132: 2809-2823, 2005.
& U; ]2 D7 _' K: z! P& T

Kobayashi A, Shawlot W, Kania A, and Behringer RR. Requirement of Lim1 for female reproductive tract development. Development 131: 539-549, 2004.+ r0 Y+ G& B0 e; z6 n# C
8 _! Y9 V. j+ ^

6 f6 e; F0 S( `0 G. `( b7 W- }
Kreidberg JA. Podocyte differentiation and glomerulogenesis. J Am Soc Nephrol 14: 806-814, 2003.

" E! @2 p! B2 K
Kreidberg JA, Sariola H, Loring JM, Maeda M, Pelletier J, Housman D, and Jaenisch R. WT-1 is required for early kidney development. Cell 74: 679-691, 1993.. T' |8 I# J3 n' k4 e% e

& @, f" L5 F+ s# s

Kume T, Deng K, and Hogan BL. Murine forkhead/winged helix genes Foxc1 (Mf1) and Foxc2 (Mfh1) are required for the early organogenesis of the kidney and urinary tract. Development 127: 1387-1395, 2000.
7 Z. _0 K' q+ l$ L# a. ]& l
+ y* P1 W4 l; y- }  V

Levinson R and Mendelsohn C. Stromal progenitors are important for patterning epithelial and mesenchymal cell types in the embryonic kidney. Semin Cell Dev Biol 14: 225-231, 2003.2 D$ L  S+ ]% A* a$ a% d
. q1 M$ ^2 @, @
6 }3 y4 L2 Y! a6 g* {* W

Levinson RS, Batourina E, Choi C, Vorontchikhina M, Kitajewski J, and Mendelsohn CL. Foxd1-dependent signals control cellularity in the renal capsule, a structure required for normal renal development. Development 132: 529-539, 2005.

7 R, q0 \7 E5 h$ Z. x; w( t: y
Li X, Oghi KA, Zhang J, Krones A, Bush KT, Glass CK, Nigam SK, Aggarwal AK, Maas R, Rose DW, and Rosenfeld MG. Eya protein phosphatase activity regulates Six1-Dach-Eya transcriptional effects in mammalian organogenesis. Nature 426: 247-254, 2003.

# z6 S8 K4 z/ d* h* J' z' Z9 e

Mansouri A, Chowdhury K, and Gruss P. Follicular cells of the thyroid gland require Pax8 gene function. Nat Genet 19: 87-90, 1998.

5 D; m8 f3 Z% t2 y1 r) f

Mendelsohn C, Batourina E, Fung S, Gilbert T, and Dodd J. Stromal cells mediate retinoid-dependent functions essential for renal development. Development 126: 1139-1148, 1999.- c' R4 F0 p$ ~4 Q& k0 o. m

# M+ K5 s+ \' M8 K8 R
Nishinakamura R, Matsumoto Y, Nakao K, Nakamura K, Sato A, Copeland NG, Gilbert DJ, Jenkins NA, Scully S, Lacey DL, Katsuki M, Asashima M, and Yokota T. Murine homolog of SALL1 is essential for ureteric bud invasion in kidney development. Development 128: 3105-3115, 2001.2 }! R& K) P4 O" ^6 C( G. S0 [- m4 c
" h+ u9 s9 J, Q3 N
* o3 q# A; G5 O2 ~2 l! w
- L" z) h. u! z1 x- y& o9 A6 B$ \4 `2 c
Obara-Ishihara T, Kuhlman J, Niswander L, and Herzlinger D. The surface ectoderm is essential for nephric duct formation in intermediate mesoderm. Development 126: 1103-1108, 1999.

; J% e- X, @" z5 n( e6 _- ?8 l
  _! K4 I$ b: K6 W3 `
Ohto H, Kamada S, Tago K, Tominaga SI, Ozaki H, Sato S, and Kawakami K. Cooperation of six and eya in activation of their target genes through nuclear translocation of Eya. Mol Cell Biol 19: 6815-6824, 1999.( _' h2 c9 Y$ e' d$ O' h% E/ Z4 b3 q

2 O; K6 c% h( `1 g
Piscione TD and Rosenblum ND. The molecular control of renal branching morphogenesis: current knowledge and emerging insights. Differentiation 70: 227-246, 2002.% X, S/ E) @1 H& Z" h0 E
2 R, _9 [) e, V3 X. G

Plaza S, Prince F, Jaeger J, Kloter U, Flister S, Benassayag C, Cribbs D, and Gehring WJ. Molecular basis for the inhibition of Drosophila eye development by Antennapedia. EMBO J 20: 802-811, 2001./ L$ \2 [1 |  Z
, `) {& T2 c5 ?% K' d
$ v8 v' V3 F, n$ L
: a* ^0 M: v7 f# w, q* c) x4 v3 n
Sainio K, Suvanto P, Davies J, Wartiovaara J, Wartiovaara K, Saarma M, Arumae U, Meng X, Lindahl M, Pachnis V, and Sariola H. Glial-cell-line-derived neurotrophic factor is required for bud initiation from ureteric epithelium. Development 124: 4077-4087, 1997.
+ E/ X- e1 ~$ u+ N9 z- l  Z7 H7 D

# e% ?! U" K! m! A. R$ }) \% l) H
Sajithlal G, Zou D, Silvius D, and Xu PX. Eya 1 acts as a critical regulator for specifying the metanephric mesenchyme. Dev Biol 284: 323-336, 2005.2 j& q! L4 c. ?* J# `" g- l: G

7 Q! o0 m% V- @# U9 `* w3 r

Sariola H. Nephron induction revisited: from caps to condensates. Curr Opin Nephrol Hypertens 11: 17-21, 2002.

Schnabel CA, Godin RE, and Cleary ML. Pbx1 regulates nephrogenesis and ureteric branching in the developing kidney. Dev Biol 254: 262-276, 2003.
) W4 x1 A& k- s8 b2 `; T3 O% l
- _8 g# ~1 `; t2 O
% V. w3 i: q8 o" ^- j; x1 }% K2 y
Shakya R, Watanabe T, and Costantini F. The role of GDNF/Ret signaling in ureteric bud cell fate and branching morphogenesis. Dev Cell 8: 65-74, 2005.

1 I' k/ |& Z  O" ?+ W
% ?+ O1 j  U: h; B1 R
Shawlot W and Behringer RR. Requirement for Lim1 in head-organizer function. Nature 374: 425-430, 1995.
9 c! e* m2 A1 w  ^; n" `, ?) {9 F

Stark K, Vainio S, Vassileva G, and McMahon AP. Epithelial transformation of metanephric mesenchyme in the developing kidney regulated by Wnt-4. Nature 372: 679-683, 1994.

Torres M, Gomez-Pardo E, Dressler GR, and Gruss P. Pax-2 controls multiple steps of urogenital development. Development 121: 4057-4065, 1995.

Treisman JE. A conserved blueprint for the eye? Bioessays 21: 843-850, 1999. <a href="/cgi/external_ref?access_num=10.1002/(SICI)1521-1878(199910)21:107 W1 [" ~) J2 H* Q7 u5 S

, P) v, E. x) X# U# L( h+ t
Tsang TE, Shawlot W, Kinder SJ, Kobayashi A, Kwan KM, Schughart K, Kania A, Jessell TM, Behringer RR, and Tam PP. Lim1 activity is required for intermediate mesoderm differentiation in the mouse embryo. Dev Biol 223: 77-90, 2000.

( U7 p5 u0 J  m
* x* H; q3 ^6 T
Vize PD, Seufert DW, Carroll TJ, and Wallingford JB. Model systems for the study of kidney development: use of the pronephros in the analysis of organ induction and patterning. Dev Biol 188: 189-204, 1997.
  ^& D* Z* U+ s% `4 T: I

, U) j+ M' `) y9 D
Vize PD, Woolf AS, and Bard JBL. The Kidney: From Normal Development to Congenital Diseases. Amsterdam: Academic, 2002.

$ Z  p/ z, E2 S  O% Q2 M# ~
3 f% ~3 G$ P& o2 }" ?
Wellik DM, Hawkes PJ, and Capecchi MR. Hox11 paralogous genes are essential for metanephric kidney induction. Genes Dev 16: 1423-1432, 2002.5 ~. G+ B7 O! |- m) Z/ ]* w2 v
( ~- N- ~/ X5 @5 j8 P8 K- D7 {+ l
  E: i: r0 R! c7 ]

Xu PX, Adams J, Peters H, Brown MC, Heaney S, and Maas R. Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia. Nat Genet 23: 113-117, 1999.

Xu PX, Zheng W, Huang L, Maire P, Laclef C, and Silvius D. Six1 is required for the early organogenesis of mammalian kidney. Development 130: 3085-3094, 2003.

$ k+ j% x( a9 w: K) y
8 V1 `0 C% T" j& C
Xu PX, Zheng W, Laclef C, Maire P, Maas RL, Peters H, and Xu X. Eya1 is required for the morphogenesis of mammalian thymus, parathyroid and thyroid. Development 129: 3033-3044, 2002.

/ |: d7 w( {3 T+ ?
Yu J, McMahon AP, and Valerius MT. Recent genetic studies of mouse kidney development. Curr Opin Genet Dev 14: 550-557, 2004.

收藏0 分享0 顶0 踩0