Loss of sequences 3′ to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination

K. McElreavey, E. Vilain, S. Barbaux, John Fuqua, P. Y. Fechner, N. Souleyreau, M. Doco-Fenzy, R. Gabriel, C. Quereux, M. Fellous, G. D. Berkovitz

Research output: Contribution to journalArticle

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Abstract

The condition termed 46,XY complete gonadal dysgenesis is characterized by a completely female phenotype and streak gonads. In contrast, subjects with 46,XY partial gonadal dysgenesis and those with embryonic testicular regression sequence usually present ambiguous genitalia and a mix of Müllerian and Wolffian structures. In 46,XY partial gonadal dysgenesis gonadal histology shows evidence of incomplete testis determination. In 46,XY embryonic testicular regression sequence there is lack of gonadal tissue on both sides. Various lines of evidence suggest that embryonic testicular regression sequence is a variant form of 46,XY gonadal dysgenesis. The sex-determining region Y chromosome gene (SKY) encodes sequences for the testis-determining factor. To date germ-line mutations in SRY have been reported in ≈20% of subjects with 46,XY complete gonadal dysgenesis. However no germ-line mutations of SRY have been reported in subjects with the partial forms. We studied 20 subjects who presented either 46,XY partial gonadal dysgenesis or 46,XY embryonic testicular regression sequence. We examined the SRY gene and the minimum region of Y-specific DNA known to confer a male phenotype. The SRY-open reading frame (ORF) was normal in all subjects. However a de novo interstitial deletion 3′ to the SRY-ORF was found in one subject. Although it is possible that the deletion was unrelated to the subject's phenotype, we propose that the deletion was responsible for the abnormal gonadal development by diminishing expression of SRY. We suggest that the deletion resulted either in the loss of sequences necessary for normal SRY expression or in a position effect that altered SRY expression. This case provides further evidence that deletions of the Y chromosome outside the SRY-ORF can result in either complete or incomplete sex reversal.

Original languageEnglish (US)
Pages (from-to)8590-8594
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume93
Issue number16
StatePublished - Aug 6 1996
Externally publishedYes

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46,XY Gonadal Dysgenesis
Testis
Open Reading Frames
Genes
Germ-Line Mutation
Phenotype
Sex-Determining Region Y Protein
sry Genes
Y-Linked Genes
Disorders of Sex Development
Gonads
Histology
Anorchia
DNA

ASJC Scopus subject areas

  • General
  • Genetics

Cite this

Loss of sequences 3′ to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination. / McElreavey, K.; Vilain, E.; Barbaux, S.; Fuqua, John; Fechner, P. Y.; Souleyreau, N.; Doco-Fenzy, M.; Gabriel, R.; Quereux, C.; Fellous, M.; Berkovitz, G. D.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 93, No. 16, 06.08.1996, p. 8590-8594.

Research output: Contribution to journalArticle

McElreavey, K, Vilain, E, Barbaux, S, Fuqua, J, Fechner, PY, Souleyreau, N, Doco-Fenzy, M, Gabriel, R, Quereux, C, Fellous, M & Berkovitz, GD 1996, 'Loss of sequences 3′ to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination', Proceedings of the National Academy of Sciences of the United States of America, vol. 93, no. 16, pp. 8590-8594.
McElreavey, K. ; Vilain, E. ; Barbaux, S. ; Fuqua, John ; Fechner, P. Y. ; Souleyreau, N. ; Doco-Fenzy, M. ; Gabriel, R. ; Quereux, C. ; Fellous, M. ; Berkovitz, G. D. / Loss of sequences 3′ to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination. In: Proceedings of the National Academy of Sciences of the United States of America. 1996 ; Vol. 93, No. 16. pp. 8590-8594.
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abstract = "The condition termed 46,XY complete gonadal dysgenesis is characterized by a completely female phenotype and streak gonads. In contrast, subjects with 46,XY partial gonadal dysgenesis and those with embryonic testicular regression sequence usually present ambiguous genitalia and a mix of M{\"u}llerian and Wolffian structures. In 46,XY partial gonadal dysgenesis gonadal histology shows evidence of incomplete testis determination. In 46,XY embryonic testicular regression sequence there is lack of gonadal tissue on both sides. Various lines of evidence suggest that embryonic testicular regression sequence is a variant form of 46,XY gonadal dysgenesis. The sex-determining region Y chromosome gene (SKY) encodes sequences for the testis-determining factor. To date germ-line mutations in SRY have been reported in ≈20{\%} of subjects with 46,XY complete gonadal dysgenesis. However no germ-line mutations of SRY have been reported in subjects with the partial forms. We studied 20 subjects who presented either 46,XY partial gonadal dysgenesis or 46,XY embryonic testicular regression sequence. We examined the SRY gene and the minimum region of Y-specific DNA known to confer a male phenotype. The SRY-open reading frame (ORF) was normal in all subjects. However a de novo interstitial deletion 3′ to the SRY-ORF was found in one subject. Although it is possible that the deletion was unrelated to the subject's phenotype, we propose that the deletion was responsible for the abnormal gonadal development by diminishing expression of SRY. We suggest that the deletion resulted either in the loss of sequences necessary for normal SRY expression or in a position effect that altered SRY expression. This case provides further evidence that deletions of the Y chromosome outside the SRY-ORF can result in either complete or incomplete sex reversal.",
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AU - Fuqua, John

AU - Fechner, P. Y.

AU - Souleyreau, N.

AU - Doco-Fenzy, M.

AU - Gabriel, R.

AU - Quereux, C.

AU - Fellous, M.

AU - Berkovitz, G. D.

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