The molecular action and regulation of the testis-determining factors, SRY (sex-determining region on the Y chromosome) and SOX9 [SRY-related high-mobility group (HMG) box 9].

Despite 12 yr since the discovery of SRY, little is known at the molecular level about how SRY and the SRY-related protein, SOX9 [SRY-related high-mobility group (HMG) box 9], initiate the program of gene expression required to commit the bipotential embryonic gonad to develop into a testis rather than an ovary. Analysis of SRY and SOX9 clinical mutant proteins and XX mice transgenic for testis-determining genes have provided some insight into their normal functions. SRY and SOX9 contain an HMG domain, a DNA-binding motif. The HMG domain plays a central role, being highly conserved between species and the site of nearly all missense mutations causing XY gonadal dysgenesis. SRY and SOX9 are architectural transcription factors; their HMG domain is capable of directing nuclear import and DNA bending. Whether SRY and SOX9 activate testis-forming genes, repress ovary-forming genes, or both remains speculative until downstream DNA target genes are identified. However, factors that control SRY and SOX9 gene expression have been identified, as have a dozen sex-determining genes, allowing some of the pieces in this molecular genetic puzzle to be connected. Many genes, however, remain unidentified, because in the majority of cases of XY females and in all cases of XX males lacking SRY, the mutated gene is unknown.

[1]  W. Vogel,et al.  Absence of Sry in species of the vole Ellobius , 1995, Nature Genetics.

[2]  P. Ridgway,et al.  The binding of a Fos/Jun heterodimer can completely disrupt the structure of a nucleosome , 1997, The EMBO journal.

[3]  Andy Greenfield,et al.  The Sry-related gene Sox9 is expressed during chondrogenesis in mouse embryos , 1995, Nature Genetics.

[4]  A. Sinclair,et al.  Genetic evidence equating SRY and the testis-determining factor , 1990, Nature.

[5]  Gerd Scherer,et al.  Direct Interaction of SRY-Related Protein SOX9 and Steroidogenic Factor 1 Regulates Transcription of the Human Anti-Müllerian Hormone Gene , 1998, Molecular and Cellular Biology.

[6]  P. Goodfellow,et al.  Rapid sequence evolution of the mammalian sex-determining gene SRY , 1993, Nature.

[7]  W. Shen,et al.  The nuclear receptor steroidogenic factor 1 acts at multiple levels of the reproductive axis. , 1994, Genes & development.

[8]  R. Teasdale,et al.  Twenty pairs of sox: extent, homology, and nomenclature of the mouse and human sox transcription factor gene families. , 2002, Developmental cell.

[9]  V. Harley,et al.  The DNA-binding specificity of SOX9 and other SOX proteins. , 1999, Nucleic acids research.

[10]  W. Gerald,et al.  The Wilms Tumor Suppressor WT1 Encodes a Transcriptional Activator of amphiregulin , 1999, Cell.

[11]  P. Goodfellow,et al.  Expression of Sry, the mouse sex determining gene. , 1995, Development.

[12]  P. Goodfellow,et al.  Evidence to exclude SOX9 as a candidate gene for XY sex reversal without skeletal malformation. , 1996, Journal of medical genetics.

[13]  S. Schneider,et al.  Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[14]  V. Harley,et al.  Differential expression of SOX9 in gonads of the sea turtle Lepidochelys olivacea at male- or female-promoting temperatures. , 1999, The Journal of experimental zoology.

[15]  Y. Seino,et al.  Acampomelic campomelic syndrome and sex reversal associated with de novo t(12;17) translocation. , 1995, American journal of medical genetics.

[16]  V. Harley,et al.  Biochemical defects in eight SRY missense mutations causing XY gonadal dysgenesis. , 2002, Molecular genetics and metabolism.

[17]  J. Bowles,et al.  New clues to the puzzle of mammalian sex determination , 2001, Genome Biology.

[18]  Peter Goodfellow,et al.  "Male Development of Chromosomally Female Mice Transgenic for Sry gene" (1991), by Peter Koopman, et al. , 2014 .

[19]  R. Behringer,et al.  Analysis of the role of Amh and Fra1 in the Sry regulatory pathway , 1996, Molecular reproduction and development.

[20]  D. Housman,et al.  A Mammal-Specific Exon of WT1 Is Not Required for Development or Fertility , 2002, Molecular and Cellular Biology.

[21]  P. Koopman,et al.  Sry and Sox9: mammalian testis-determining genes , 1999, Cellular and Molecular Life Sciences CMLS.

[22]  L. Bolund,et al.  Assignment of an autosomal sex reversa– locus (SRA1) and campomelic dysplasia (CMPD1) to 17q24.3–q25.1 , 1993, Nature Genetics.

[23]  T. Matsuzawa,et al.  The Primates , 1957, Nature.

[24]  O. Birk,et al.  The LIM homeobox gene Lhx9 is essential for mouse gonad formation , 2000, Nature.

[25]  E. Vilain,et al.  Characterization and sequence of the 5' flanking region of the human testis-determining factor SRY , 1992 .

[26]  Yun-Fai Chris Lau,et al.  Identification of the transcriptional unit, structural organization, and promoter sequence of the human sex-determining region Y (SRY) gene, using a reverse genetic approach. , 1993, American journal of human genetics.

[27]  J. Jameson,et al.  Gonadal determination and adrenal development are regulated by the orphan nuclear receptor steroidogenic factor-1, in a dose-dependent manner. , 2002, The Journal of clinical endocrinology and metabolism.

[28]  D. Higgs,et al.  The alpha-thalassemia/mental retardation syndromes. , 1996, Medicine.

[29]  Jobst Meyer,et al.  Translocation breakpoints in three patients with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9 , 1996, Human Genetics.

[30]  Sahar Mansour,et al.  Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene , 1994, Nature.

[31]  O. Bachs,et al.  Calmodulin and calmodulin-binding proteins in the nucleus. , 1994, Cell calcium.

[32]  J. Bowles,et al.  Regulation of male sexual development by Sry and Sox9. , 2001, The Journal of experimental zoology.

[33]  N. Lamb,et al.  Nuclear localization of the testis determining gene product SRY , 1995, The Journal of cell biology.

[34]  P. Sharpe,et al.  The evolution of WT1 sequence and expression pattern in the vertebrates. , 1995, Oncogene.

[35]  H. Ostrer,et al.  Sry is a transcriptional activator. , 1994, Molecular endocrinology.

[36]  C. Chuong,et al.  Activation of protein kinase A is a pivotal step involved in both BMP‐2‐ and cyclic AMP‐induced chondrogenesis , 1997, Journal of cellular physiology.

[37]  Anwar Hossain,et al.  The Human Sex-determining Gene SRY Is a Direct Target of WT1 * , 2001, The Journal of Biological Chemistry.

[38]  G. Scherer,et al.  Two Independent Nuclear Localization Signals Are Present in the DNA-binding High-mobility Group Domains of SRY and SOX9* , 1997, The Journal of Biological Chemistry.

[39]  J. Martín,et al.  prx-1 functions cooperatively with another paired-related homeobox gene, prx-2, to maintain cell fates within the craniofacial mesenchyme. , 1999, Development.

[40]  B. Capel,et al.  Sry induces cell proliferation in the mouse gonad. , 2000, Development.

[41]  Z. Wang,et al.  WT1, the Wilms' tumor suppressor gene product, represses transcription through an interactive nuclear protein. , 1995, Oncogene.

[42]  D. Ornitz,et al.  Male-to-Female Sex Reversal in Mice Lacking Fibroblast Growth Factor 9 , 2001, Cell.

[43]  A. Sinclair,et al.  The human SRY transcript. , 1993, Human molecular genetics.

[44]  B. Roe,et al.  The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factor , 1998, Human Genetics.

[45]  P. de Santa Barbara,et al.  Expression and subcellular localization of SF‐1, SOX9, WT1, and AMH proteins during early human testicular development , 2000, Developmental dynamics : an official publication of the American Association of Anatomists.

[46]  P. Walsh,et al.  WT1: what has the last decade told us? , 1999, BioEssays : news and reviews in molecular, cellular and developmental biology.

[47]  J. Tremblay,et al.  GATA factors differentially activate multiple gonadal promoters through conserved GATA regulatory elements. , 2001, Endocrinology.

[48]  M. Mattei,et al.  Early expression of AMH in chicken embryonic gonads precedes testicular SOX9 expression , 1998, Developmental dynamics : an official publication of the American Association of Anatomists.

[49]  E. Eicher,et al.  Sex reversal in C57BL/6J-YPOS mice corrected by a Sry transgene. , 1995, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[50]  C. Ferraz,et al.  Comparative genomics of the SOX9 region in human and Fugu rubripes: conservation of short regulatory sequence elements within large intergenic regions. , 2001, Genomics.

[51]  P. Goodfellow,et al.  The SRY protein, like HMG 1, recognizes (CA)n sequences, an abundant repeat sequence in vertebrates. , 1995, Biochemistry and molecular biology international.

[52]  I. Barroso,et al.  Compound Effects of Point Mutations Causing Campomelic Dysplasia/Autosomal Sex Reversal upon SOX9 Structure, Nuclear Transport, DNA Binding, and Transcriptional Activation* , 2001, The Journal of Biological Chemistry.

[53]  Véronique Lefebvre,et al.  A new long form of Sox5 (L‐Sox5), Sox6 and Sox9 are coexpressed in chondrogenesis and cooperatively activate the type II collagen gene , 1998, The EMBO journal.

[54]  B. Birren,et al.  Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region. , 1999, American journal of human genetics.

[55]  P. Koopman,et al.  Cloning and characterisation of the Sry-related transcription factor gene Sox8. , 2000, Nucleic acids research.

[56]  W. Shen,et al.  Nuclear receptor steroidogenic factor 1 regulates the müllerian inhibiting substance gene: A link to the sex determination cascade , 1994, Cell.

[57]  K. Wertz,et al.  Large-scale screen for genes involved in gonad development , 2000, Mechanisms of Development.

[58]  Robin Lovell-Badge,et al.  A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif , 1990, Nature.

[59]  V. Lefebvre,et al.  Erratum: Phosphorylation of SOX9 by cyclic AMP-dependent protein kinase a enhances SOX9's ability to transactivate a Col2a1 chondrocyte-specific enhancer (Molecular and Cellular Biology (2000) 20:11 (p. 4149-4158)) , 2000 .

[60]  M. Soares,et al.  Sexually dimorphic expression of protease nexin-1 and vanin-1 in the developing mouse gonad prior to overt differentiation suggests a role in mammalian sexual development. , 2000, Human molecular genetics.

[61]  K. H. Albrecht,et al.  Evidence that Sry is expressed in pre-Sertoli cells and Sertoli and granulosa cells have a common precursor. , 2001, Developmental biology.

[62]  K. Parker,et al.  A cell-specific nuclear receptor is essential for adrenal and gonadal development and sexual differentiation , 1994, Cell.

[63]  Y. Ning,et al.  Autosomal XX sex reversal caused by duplication of SOX9. , 1999, American journal of medical genetics.

[64]  P. Goodfellow,et al.  A familial mutation in the testis-determining gene SRY shared by both sexes , 1992, Human Genetics.

[65]  F. Heitz,et al.  Description and functional implications of a novel mutation in the sex‐determining gene SRY , 1994, Human mutation.

[66]  P N Goodfellow,et al.  DNA binding activity of recombinant SRY from normal males and XY females. , 1992, Science.

[67]  P. Jacobs,et al.  A Case of Human Intersexuality Having a Possible XXY Sex-Determining Mechanism , 1959, Nature.

[68]  J. Beckmann,et al.  The region on 9p associated with 46,XY sex reversal contains several transcripts expressed in the urogenital system and a novel doublesex-related domain. , 2000, Genomics.

[69]  Richard R. Behringer,et al.  Sox9 is required for cartilage formation , 1999, Nature Genetics.

[70]  J. Forwood,et al.  Defective importin β recognition and nuclear import of the sex-determining factor SRY are associated with XY sex-reversing mutations , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[71]  E. Vilain,et al.  XY sex reversal associated with a deletion 5' to the SRY "HMG box" in the testis-determining region. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[72]  V. Vidal,et al.  Sox9 induces testis development in XX transgenic mice , 2001, Nature Genetics.

[73]  K. Jones,et al.  Testis development in a mouse with 10% of XY cells. , 1987, Developmental biology.

[74]  K. Vass,et al.  A novel missense mutation (S18N) in the 5′ non-HMG box region of the SRY gene in a patient with partial gonadal dysgenesis and his normal male relatives , 1998, Human Genetics.

[75]  P. Burgoyne Role of mammalian Y chromosome in sex determination. , 1988, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[76]  P. Koopman,et al.  Structural and functional characterization of the mouse Sox9 promoter: implications for campomelic dysplasia. , 1999, Human molecular genetics.

[77]  R Grosschedl,et al.  HMG domain proteins: architectural elements in the assembly of nucleoprotein structures. , 1994, Trends in genetics : TIG.

[78]  R. Veitia,et al.  Conservation of Y chromosome-specific sequences immediately 5' to the testis determining gene in primates. , 1997, Gene.

[79]  A. Means,et al.  Calmodulin and the cell cycle: Involvement in regulation of cell-cycle progression , 1982, Cell.

[80]  P. Goodfellow,et al.  Definition of a consensus DNA binding site for SRY. , 1994, Nucleic acids research.

[81]  A. Mclaren,et al.  Germ cells and germ cell sex. , 1995, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[82]  S. Lynch,et al.  Campomelic dysplasia: evidence of autosomal dominant inheritance. , 1993, Journal of medical genetics.

[83]  V. Laudet,et al.  Diversification Pattern of the HMG and SOX Family Members During Evolution , 1999, Journal of Molecular Evolution.

[84]  J. Hall,et al.  Transactivation of the WT1 antisense promoter is unique to the WT1[+/−] isoform , 1999, FEBS letters.

[85]  Robin Lovell-Badge,et al.  Targeted Mutagenesis of the Endogenous Mouse Mis Gene Promoter In Vivo Definition of Genetic Pathways of Vertebrate Sexual Development , 1999, Cell.

[86]  Frank Grosveld,et al.  Transcription Factor Sp1 Is Essential for Early Embryonic Development but Dispensable for Cell Growth and Differentiation , 1997, Cell.

[87]  G. Giuili,et al.  The nuclear receptor SF-1 mediates sexually dimorphic expression of Mullerian Inhibiting Substance, in vivo. , 1997, Development.

[88]  M. Newbould,et al.  Phenotypic diversity in the Smith‐Lemli‐Opitz syndrome , 1997, Clinical dysmorphology.

[89]  P. Démoulin,et al.  Ju n 20 07 Progressive transformation of a flux rope to an ICME Comparative analysis using the direct and fitted expansion methods , 2008 .

[90]  J. W. Foster,et al.  Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal. , 1995, American journal of human genetics.

[91]  J. Licht,et al.  Tumor-associated WT1 Missense Mutants Indicate That Transcriptional Activation by WT1 Is Critical for Growth Control* , 1999, The Journal of Biological Chemistry.

[92]  J. Hanover,et al.  Calmodulin activates nuclear protein import: a link between signal transduction and nuclear transport. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[93]  P N Goodfellow,et al.  SRY, like HMG1, recognizes sharp angles in DNA. , 1992, The EMBO journal.

[94]  S. Ranganathan,et al.  Functional and Structural Studies of Wild Type SOX9 and Mutations Causing Campomelic Dysplasia* , 1999, The Journal of Biological Chemistry.

[95]  P. Donahoe,et al.  Molecular basis of mammalian sexual determination: activation of Müllerian inhibiting substance gene expression by SRY. , 1994, Science.

[96]  David I. Wilson,et al.  SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development , 2000, Mechanisms of Development.

[97]  P. de Santa Barbara,et al.  Characterization of two Sp1 binding sites of the human sex determining SRY promoter. , 1998, Biochimica et biophysica acta.

[98]  A. Greenfield Applications of DNA microarrays to the transcriptional analysis of mammalian genomes , 2000, Mammalian Genome.

[99]  V. Vidal,et al.  Early gonadal development: exploring Wt1 and Sox9 function. , 2002, Novartis Foundation symposium.

[100]  Owen J. Marshall,et al.  Identification of an interaction between SOX9 and HSP70 , 2001, FEBS letters.

[101]  E. Vilain,et al.  Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[102]  V. Harley The molecular action of testis-determining factors SRY and SOX9. , 2002, Novartis Foundation symposium.

[103]  R. Lovell-Badge,et al.  Dax1 antagonizes Sry action in mammalian sex determination , 1998, Nature.

[104]  I. Herskowitz,et al.  A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[105]  Gerd Scherer,et al.  Sex reversal by loss of the C–terminal transactivation domain of human SOX9 , 1996, Nature Genetics.

[106]  P. de Santa Barbara,et al.  Steroidogenic Factor-1 Contributes to the Cyclic-Adenosine Monophosphate Down-Regulation of Human SRY Gene Expression1 , 2001, Biology of reproduction.

[107]  J. Bowles,et al.  A subtractive gene expression screen suggests a role for vanin‐1 in testis development in mice , 2000, Genesis.

[108]  V. Lefebvre,et al.  Potent Inhibition of the Master Chondrogenic FactorSox9 Gene by Interleukin-1 and Tumor Necrosis Factor-α* , 2000, The Journal of Biological Chemistry.

[109]  A. McMahon,et al.  Female development in mammals is regulated by Wnt-4 signalling , 1999, Nature.

[110]  G. Scherer The molecular genetic jigsaw puzzle of vertebrate sex determination and its missing pieces. , 2002, Novartis Foundation symposium.

[111]  N. Hastie,et al.  Life, Sex, and WT1 Isoforms— Three Amino Acids Can Make All the Difference , 2001, Cell.

[112]  C. S. Raymond,et al.  Evidence for evolutionary conservation of sex-determining genes , 1998, Nature.

[113]  B. Capel,et al.  Three-dimensional structure of the developing mouse genital ridge. , 1995, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[114]  A. Schedl,et al.  YAC complementation shows a requirement for Wt1 in the development of epicardium, adrenal gland and throughout nephrogenesis. , 1999, Development.

[115]  A. Sinclair,et al.  Mutation analysis of the SOX9 gene in a patient with campomelic dysplasia , 1998, Human mutation.

[116]  M. Goebl,et al.  DNA-binding properties of the product of the testis-determining gene and a related protein , 1991, Nature.

[117]  Y. Yan,et al.  Two sox9 genes on duplicated zebrafish chromosomes: expression of similar transcription activators in distinct sites. , 2001, Developmental biology.

[118]  Y. Aslan,et al.  Campomelic dysplasia associated with mandibular clefting. , 1996, Genetic counseling.

[119]  E. Vilain,et al.  Dimerization of SOX9 is required for chondrogenesis, but not for sex determination. , 2003, Human molecular genetics.

[120]  A. Monaco,et al.  An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita , 1994, Nature.

[121]  J. Pelletier,et al.  The Wilms’ Tumor Suppressor Gene (wt1) Product Regulates Dax-1 Gene Expression during Gonadal Differentiation , 1999, Molecular and Cellular Biology.

[122]  V. Lefebvre,et al.  Three High Mobility Group-like Sequences within a 48-Base Pair Enhancer of the Col2a1 Gene Are Required for Cartilage-specific Expression in Vivo * , 1998, The Journal of Biological Chemistry.

[123]  P N Goodfellow,et al.  SRY and sex determination in mammals. , 1993, Annual review of genetics.

[124]  P. Donahoe,et al.  An SRY mutation causing human sex reversal resolves a general mechanism of structure-specific DNA recognition: application to the four-way DNA junction. , 1995, Biochemistry.

[125]  P N Goodfellow,et al.  Deletion of long-range regulatory elements upstream of SOX9 causes campomelic dysplasia. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[126]  R. Lovell-Badge,et al.  Expression of a candidate sex-determining gene during mouse testis differentiation , 1990, Nature.

[127]  Y. Nakamura,et al.  Isolation of a testis-specific cDNA on chromosome 17q from a region adjacent to the breakpoint of t(12;17) observed in a patient with acampomelic campomelic dysplasia and sex reversal. , 1996, Human molecular genetics.

[128]  J. Licht,et al.  WT1-mediated Transcriptional Activation Is Inhibited by Dominant Negative Mutant Proteins (*) , 1995, The Journal of Biological Chemistry.

[129]  H. Burtscher,et al.  BMP-2 and sonic hedgehog have contrary effects on adipocyte-like differentiation of C3H10T1/2 cells. , 2000, DNA and cell biology.

[130]  C. E. Ford,et al.  A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome). , 1959, Lancet.

[131]  Paul A. Overbeek,et al.  A transgenic insertion upstream of Sox9 is associated with dominant XX sex reversal in the mouse , 2000, Nature Genetics.

[132]  P. McDonough,et al.  Analysis of DNA binding activity of the recombinant SRY protein from xy sex reversed females mutant for SRY (n = 4) , 1998 .

[133]  H. Kondoh,et al.  Mechanism of Regulatory Target Selection by the SOX High-Mobility-Group Domain Proteins as Revealed by Comparison of SOX1/2/3 and SOX9 , 1999, Molecular and Cellular Biology.

[134]  E. Vilain Anomalies of human sexual development: clinical aspects and genetic analysis. , 2002, Novartis Foundation symposium.

[135]  S Sakano,et al.  Trans‐activation of the Mouse Cartilage‐Derived Retinoic Acid‐Sensitive Protein Gene by Sox9 , 1999, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[136]  S. E. Hall,et al.  Sequence and expression analysis of WT1 and Sox9 in the red-eared slider turtle, Trachemys scripta. , 1998, The Journal of experimental zoology.

[137]  C. S. Raymond,et al.  Dmrt1, a gene related to worm and fly sexual regulators, is required for mammalian testis differentiation. , 2000, Genes & development.

[138]  Eric Vilain,et al.  Familial mutation in the testis-determining gene SRY shared by an XY female and her normal father. , 2002, The Journal of clinical endocrinology and metabolism.

[139]  C. Tyler-Smith,et al.  Mutation analysis of the 2 kb 5' to SRY in XY females and XY intersex subjects. , 1996, Journal of medical genetics.

[140]  K. H. Albrecht,et al.  Related function of mouse SOX3, SOX9, and SRY HMG domains assayed by male sex determination , 2000, Genesis.

[141]  J. Bowles,et al.  Sry requires a CAG repeat domain for male sex determination in Mus musculus , 1999, Nature Genetics.

[142]  B. Bardoni,et al.  Two novel SRY missense mutations reducing DNA binding identified in XY females and their mosaic fathers. , 1995, American journal of human genetics.

[143]  R. Lovell-Badge,et al.  Mammalian sex determination: a molecular drama. , 1999, Genes & development.

[144]  F. Rauscher,et al.  The WT1 Wilms tumor gene product: a developmentally regulated transcription factor in the kidney that functions as a tumor suppressor , 1993, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[145]  J. Licht,et al.  A novel repressor, par-4, modulates transcription and growth suppression functions of the Wilms' tumor suppressor WT1 , 1996, Molecular and cellular biology.

[146]  P. Rossi,et al.  Direct evidence that the mouse sex‐determining gene Sry is expressed in the somatic cells of male fetal gonads and in the germ cell line in the adult testis , 1993, Molecular reproduction and development.

[147]  R Grosschedl,et al.  Distinct DNA-binding properties of the high mobility group domain of murine and human SRY sex-determining factors. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[148]  M. Pembrey,et al.  A clinical and genetic study of campomelic dysplasia. , 1995, Journal of medical genetics.

[149]  K. Ohe,et al.  Orphan Receptor DAX-1 Is a Shuttling RNA Binding Protein Associated with Polyribosomes via mRNA , 2000, Molecular and Cellular Biology.

[150]  P. Goodfellow,et al.  Mutational analysis of SRY: nonsense and missense mutations in XY sex reversal , 1992, Human Genetics.

[151]  R. Lovell-Badge,et al.  Sex‐reversing mutations affect the architecture of SRY‐DNA complexes. , 1994, The EMBO journal.

[152]  D. Richard,et al.  Par4 is a coactivator for a splice isoform-specific transcriptional activation domain in WT1. , 2001, Genes & development.

[153]  N. Tommerup,et al.  Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9 , 1994, Cell.

[154]  A. Sinclair,et al.  Mutations in SRY and SOX9: Testis‐determining genes , 1997, Human mutation.

[155]  A. Clayton,et al.  A SOX9 Defect of Calmodulin-dependent Nuclear Import in Campomelic Dysplasia/Autosomal Sex Reversal* , 2003, Journal of Biological Chemistry.

[156]  P. Goodfellow,et al.  Sox9 expression during gonadal development implies a conserved role for the gene in testis differentiation in mammals and birds , 1996, Nature Genetics.

[157]  David Housman,et al.  WT-1 is required for early kidney development , 1993, Cell.

[158]  J. Martín,et al.  The paired-like homeo box gene MHox is required for early events of skeletogenesis in multiple lineages. , 1995, Genes & development.

[159]  L. B. Russell,et al.  THE Y-CHROMOSOME AS THE BEARER OF MALE DETERMINING FACTORS IN THE MOUSE. , 1959, Proceedings of the National Academy of Sciences of the United States of America.

[160]  P. Koopman,et al.  Spatially dynamic expression of Sry in mouse genital ridges , 2001, Developmental dynamics : an official publication of the American Association of Anatomists.

[161]  P. Jay,et al.  Phosphorylation of an N-terminal Motif Enhances DNA-binding Activity of the Human SRY Protein* , 1998, The Journal of Biological Chemistry.

[162]  G. Scherer,et al.  Three novel SRY mutations in XY gonadal dysgenesis and the enigma of XY gonadal dysgenesis cases without SRY mutations , 1998, Cytogenetic and Genome Research.

[163]  A. Schedl,et al.  Two Splice Variants of the Wilms' Tumor 1 Gene Have Distinct Functions during Sex Determination and Nephron Formation , 2001, Cell.

[164]  B. Schimmer,et al.  Steroidogenic factor 1: a key determinant of endocrine development and function. , 1997, Endocrine reviews.

[165]  P. Hindmarsh,et al.  A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans , 1999, Nature Genetics.

[166]  A. Sinclair,et al.  SRY protein enhances transcription of Fos-related antigen 1 promoter constructs. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[167]  O. Haas,et al.  Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlations. , 1997, Human molecular genetics.

[168]  R. Ezzell,et al.  Inhibition of cellular proliferation by the Wilms tumor suppressor WT1 requires association with the inducible chaperone Hsp70. , 1998, Genes & development.

[169]  R. Lovell-Badge,et al.  Sex-determining genes in mice: building pathways. , 2002, Novartis Foundation symposium.

[170]  関矢 一郎 SOX9 Enhances Aggrecan Gene Promoter/Enhancer Activity and Is Up-regulated by Retinoic Acid in a Cartilage-Derived Cell Line,TC6 , 2000 .

[171]  J. Perchellet,et al.  Studies on sex differentiation in mammals. , 1973, Recent progress in hormone research.

[172]  D. Chadwick,et al.  The genetics and biology of sex determination , 2002 .

[173]  Donald M. Bell,et al.  SOX9 binds DNA, activates transcription, and coexpresses with type II collagen during chondrogenesis in the mouse. , 1997, Developmental biology.

[174]  M. Desclozeaux,et al.  The Human Testis Determining Factor SRY Binds a Nuclear Factor Containing PDZ Protein Interaction Domains* , 1997, The Journal of Biological Chemistry.

[175]  P N Goodfellow,et al.  SOX9 is a potent activator of the chondrocyte-specific enhancer of the pro alpha1(II) collagen gene , 1997, Molecular and cellular biology.

[176]  Patrick P.L. Tam,et al.  SOX9 directly regulates the type-ll collagen gene , 1997, Nature Genetics.

[177]  T. Zwingman,et al.  Transcription of the sex-determining region genes Sry and Zfy in the mouse preimplantation embryo. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[178]  J. Bowles,et al.  Mouse SRY requires a CAG repeat domain for male sex determination. , 1999 .

[179]  A. Gronenborn,et al.  NMR spectroscopic analysis of the DNA conformation induced by the human testis determining factor SRY. , 1995, Biochemistry.

[180]  K. Ohe,et al.  A direct role of SRY and SOX proteins in pre-mRNA splicing , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[181]  X. Chen,et al.  Up-regulation of WNT-4 signaling and dosage-sensitive sex reversal in humans. , 2001, American journal of human genetics.

[182]  T. Yanase,et al.  Dax-1 as one of the target genes of Ad4BP/SF-1. , 1999, Molecular endocrinology.

[183]  E. Eicher,et al.  Inherited sex reversal in mice: identification of a new primary sex-determining gene. , 1983, The Journal of experimental zoology.

[184]  P. Maderson,et al.  Growth and differentiation of skin. , 1976, The Journal of investigative dermatology.

[185]  R. Oliva,et al.  Identification of conserved potentially regulatory sequences of the SRY gene from 10 different species of mammals. , 1998, Biochemical and biophysical research communications.

[186]  A. Sinclair,et al.  Temperature‐dependent sex determination: Upregulation of SOX9 expression after commitment to male development , 1999, Developmental dynamics : an official publication of the American Association of Anatomists.

[187]  E. Maltby,et al.  Campomelic dysplasia associated with a de novo 2q;17q reciprocal translocation. , 1992, Journal of medical genetics.

[188]  B. Capel Sex in the 90s: SRY and the switch to the male pathway. , 1998, Annual review of physiology.

[189]  S. Yamashita,et al.  Rainbow trout SOX9: cDNA cloning, gene structure and expression. , 1997, Gene.

[190]  G. Hammer,et al.  Wilms' Tumor 1 and Dax-1 Modulate the Orphan Nuclear Receptor SF-1 in Sex-Specific Gene Expression , 1998, Cell.

[191]  E. Lalli,et al.  DNA binding and transcriptional repression by DAX-1 blocks steroidogenesis , 1997, Nature.

[192]  P. Goodfellow,et al.  The HMG box of SRY is a calmodulin binding domain , 1996, FEBS letters.

[193]  P. Goodfellow,et al.  DAX-1, an ‘antitestis’gene , 1999, Cellular and Molecular Life Sciences CMLS.

[194]  F. Poulat,et al.  Steroidogenic Factor-1 Regulates Transcription of the Human Anti-müllerian Hormone Receptor* , 1998, The Journal of Biological Chemistry.

[195]  D. Zarkower Establishing sexual dimorphism: conservation amidst diversity? , 2001, Nature Reviews Genetics.