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Characterization of a new TSPY gene family member in Yq (TSPYq1)

Ratti A.a · Stuppia L.b,c · Gatta V.b · Fogh I.a · Calabrese G.b,d · Pizzuti A.a,e · Palka G.b,d
aIstituto di Clinica Neurologica, Università di Milano, Ospedale Policlinico IRCCS; bDipartimento di Scienze Biomediche, Sezione di Genetica Medica, Università “G. D’Annunzio,” Chieti; cIstituto di Citomorfologia Umana Normale e Patologica CNR, Chieti; dServizio di Genetica Umana, Ospedale Civile di Pescara; and eC.S.S.-Mendel Institute IRCCS, San Giovanni Rotondo (Italy). Cytogenet Cell Genet 88:159–162 (2000) (DOI:10.1159/000015510)

Abstract

Abstract.

We investigated subinterval 6E on the human Y chromosome, a region frequently deleted in infertile males. YAC yOX17, mapped within subinterval 6E by STS-PCR, was analyzed for the presence of new genes. TSPYq1, a member of the TSPY multi-copy gene family, was isolated and character- ized from a yOX17 cosmid subclone. PCR and FISH analysis performed on normal subjects and on patients with microdeletions of Yq suggested the presence of multiple copies of TSPY in Yq.   

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