Literature DB >> 9093193

Paternal somatic and germ-line mosaicism for a sex-determining region on Y (SRY) missense mutation leading to recurrent 46,XY sex reversal.

R S Hines1, S P Tho, Y Y Zhang, L Plouffe, K A Hansen, I Khan, P G McDonough.   

Abstract

OBJECTIVE: To determine the etiology for recurrent 46,XY sex reversal in a family with two Swyer siblings.
DESIGN: Deoxyribonucleic acid (DNA) from peripheral lymphocytes and sperm were analyzed for duplication of the dosage sensitive sex locus (DSS) and for mutations in sex-determining region on Y (SRY).
SETTING: An academic teaching hospital. PATIENTS: A family consisting of mother, father, and five phenotypic daughters, of which two were 46,XY sex-reversed females. INTERVENTION: Deoxyribonucleic acid (DNA) extraction, polymerase chain reaction (PCR), Southern blotting, dosage densitometry, single-strand conformation polymorphism (SSCP), and sequencing. MAIN OUTCOME MEASURE: Comparison of control and subject DNA.
RESULTS: Deoxyribonucleic acid (DNA) analysis of SRY in genomic DNA from the 46,XY sex-reversed siblings revealed identical missense mutations (T-->G) in both sisters. Analysis of the SRY gene in paternal lymphocyte and sperm DNA revealed mosaicism for wild and mutant (T-->G) SRY sequences. SRY analysis of sperm DNA also demonstrated the same mosaicism for the T-->G missense mutation.
CONCLUSION: A postembryonic SRY mutation gave rise to paternal mosaicism for two distinct cell populations (SRY+/SRY-). The presence of a wild type SRY in the somatic cell line may account for a normal pattern of male sexual differentiation, whereas the presence of a mutated SRY in the germ line resulted in two 46,XY sex-reversed offspring. These results confirm a proposed mechanism for the condition of recurrent 46,XY sex-reversed females.

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Year:  1997        PMID: 9093193     DOI: 10.1016/s0015-0282(97)81365-9

Source DB:  PubMed          Journal:  Fertil Steril        ISSN: 0015-0282            Impact factor:   7.329


  5 in total

1.  Familial 46,XY sex reversal without campomelic dysplasia caused by a deletion upstream of the SOX9 gene.

Authors:  Bala Bhagavath; Lawrence C Layman; Reinhard Ullmann; Yiping Shen; Kyungsoo Ha; Khurram Rehman; Stephen Looney; Paul G McDonough; Hyung-Goo Kim; Bruce R Carr
Journal:  Mol Cell Endocrinol       Date:  2014-06-04       Impact factor: 4.102

2.  A de novo phe671eu mutation in the SRY gene in a patient with complete 46,XY gonadal dysgenesis.

Authors:  J C Zenteno; S Carranza-Lira; A L Jiménez; S Kofman
Journal:  J Endocrinol Invest       Date:  2003-11       Impact factor: 4.256

3.  Failure of SOX9 regulation in 46XY disorders of sex development with SRY, SOX9 and SF1 mutations.

Authors:  Kevin C Knower; Sabine Kelly; Louisa M Ludbrook; Stefan Bagheri-Fam; Helena Sim; Pascal Bernard; Ryohei Sekido; Robin Lovell-Badge; Vincent R Harley
Journal:  PLoS One       Date:  2011-03-11       Impact factor: 3.240

Review 4.  Genetic mosaics and the germ line lineage.

Authors:  Mark E Samuels; Jan M Friedman
Journal:  Genes (Basel)       Date:  2015-04-17       Impact factor: 4.096

5.  A Rare Case of Swyer Syndrome in Two Sisters with Successful Pregnancy Outcome in Both.

Authors:  Anupam Gupta; Ritika Bajaj; Umesh N Jindal
Journal:  J Hum Reprod Sci       Date:  2019 Jul-Sep
  5 in total

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