Literature DB >> 8520965

The molecular genetics of human sex determination.

U Wolf1.   

Abstract

The classical conception of the chromosomal mechanism of sex determination presumes a chromosome unique for and determining the heterogametic sex. On the basis of recent evidence, however, this picture is becoming increasingly complex, with a multitude of genes appearing to interact simultaneously or successively to bring about the gonadal phenotype. The genes identified so far that are thought to be involved in the process of human sex determination are distributed on various chromosomes, but the consecution of their function remains to be elucidated. To the Y chromosome only a relative role can be ascribed, and it has not yet been established which gene is on top of the cascade. All of the genes under discussion are involved in transcriptional control, and at least the majority of them appear to exert pleiotropic effects. The regulation of their expression must still be defined, and it will be a long way before a link to gonadal morphogenesis is ultimately found.

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Year:  1995        PMID: 8520965     DOI: 10.1007/bf00192884

Source DB:  PubMed          Journal:  J Mol Med (Berl)        ISSN: 0946-2716            Impact factor:   4.599


  54 in total

1.  A novel mutation localized in the 3' non-HMG box region of the SRY gene in 46,XY gonadal dysgenesis.

Authors:  T Tajima; J Nakae; N Shinohara; K Fujieda
Journal:  Hum Mol Genet       Date:  1994-07       Impact factor: 6.150

2.  Evidence that the SRY protein is encoded by a single exon on the human Y chromosome.

Authors:  M A Behlke; J S Bogan; P Beer-Romero; D C Page
Journal:  Genomics       Date:  1993-09       Impact factor: 5.736

Review 3.  SRY and sex determination in mammals.

Authors:  P N Goodfellow; R Lovell-Badge
Journal:  Annu Rev Genet       Date:  1993       Impact factor: 16.830

4.  Nucleolar transcription factor hUBF contains a DNA-binding motif with homology to HMG proteins.

Authors:  H M Jantzen; A Admon; S P Bell; R Tjian
Journal:  Nature       Date:  1990-04-26       Impact factor: 49.962

5.  A regulatory cascade hypothesis for mammalian sex determination: SRY represses a negative regulator of male development.

Authors:  K McElreavey; E Vilain; N Abbas; I Herskowitz; M Fellous
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-15       Impact factor: 11.205

Review 6.  Molecular basis of mammalian sexual determination: activation of Müllerian inhibiting substance gene expression by SRY.

Authors:  C M Haqq; C Y King; E Ukiyama; S Falsafi; T N Haqq; P K Donahoe; M A Weiss
Journal:  Science       Date:  1994-12-02       Impact factor: 47.728

Review 7.  The campomelic syndrome: review, report of 17 cases, and follow-up on the currently 17-year-old boy first reported by Maroteaux et al in 1971.

Authors:  C S Houston; J M Opitz; J W Spranger; R I Macpherson; M H Reed; E F Gilbert; J Herrmann; A Schinzel
Journal:  Am J Med Genet       Date:  1983-05

8.  Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9.

Authors:  T Wagner; J Wirth; J Meyer; B Zabel; M Held; J Zimmer; J Pasantes; F D Bricarelli; J Keutel; E Hustert; U Wolf; N Tommerup; W Schempp; G Scherer
Journal:  Cell       Date:  1994-12-16       Impact factor: 41.582

9.  A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversal.

Authors:  B Bardoni; E Zanaria; S Guioli; G Floridia; K C Worley; G Tonini; E Ferrante; G Chiumello; E R McCabe; M Fraccaro
Journal:  Nat Genet       Date:  1994-08       Impact factor: 38.330

10.  A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes.

Authors:  J Gubbay; J Collignon; P Koopman; B Capel; A Economou; A Münsterberg; N Vivian; P Goodfellow; R Lovell-Badge
Journal:  Nature       Date:  1990-07-19       Impact factor: 49.962

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  1 in total

Review 1.  H-Y antigens.

Authors:  U Müller
Journal:  Hum Genet       Date:  1996-06       Impact factor: 4.132

  1 in total

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