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睾丸发育所需的人类9号染色体短臂区域包含两个与已知性调节因子相关的基因。

A region of human chromosome 9p required for testis development contains two genes related to known sexual regulators.

作者信息

Raymond C S, Parker E D, Kettlewell J R, Brown L G, Page D C, Kusz K, Jaruzelska J, Reinberg Y, Flejter W L, Bardwell V J, Hirsch B, Zarkower D

机构信息

Biochemistry, Molecular Biology and Biophysics Graduate Program, University of Minnesota, Minneapolis 55455, USA.

出版信息

Hum Mol Genet. 1999 Jun;8(6):989-96. doi: 10.1093/hmg/8.6.989.

Abstract

Deletion of the distal short arm of chromosome 9 (9p) has been reported in a number of cases to be associated with gonadal dysgenesis and XY sex reversal, suggesting that this region contains one or more genes required in two copies for normal testis development. Recent studies have greatly narrowed the interval containing this putative autosomal testis-determining gene(s) to the distal portion of 9p24.3. We previously identified DMRT1, a human gene with sequence similarity to genes that regulate the sexual development of nematodes and insects. These genes contain a novel DNA-binding domain, which we named the DM domain. DMRT1 maps to 9p24. 3 and in adults is expressed specifically in the testis. We have investigated the possible role of DM domain genes in 9p sex reversal. We identified a second DM domain gene, DMRT2, which also maps to 9p24.3. We found that point mutations in the coding region of DMRT1 and the DM domain of DMRT2 are not frequent in XY females. We showed by fluorescence in situ hybridization analysis that both genes are deleted in the smallest reported sex-reversing 9p deletion, suggesting that gonadal dysgenesis in 9p-deleted individuals might be due to combined hemizygosity of DMRT1 and DMRT2.

摘要

据报道,在许多病例中,9号染色体短臂远端(9p)的缺失与性腺发育不全和XY性反转有关,这表明该区域包含一个或多个正常睾丸发育所需的双拷贝基因。最近的研究已将包含该假定常染色体睾丸决定基因的区间大大缩小至9p24.3的远端部分。我们之前鉴定出了DMRT1,这是一个人类基因,其序列与调控线虫和昆虫性别发育的基因相似。这些基因包含一个新的DNA结合结构域,我们将其命名为DM结构域。DMRT1定位于9p24.3,在成年人中仅在睾丸中表达。我们研究了DM结构域基因在9p性反转中的可能作用。我们鉴定出了第二个DM结构域基因DMRT2,它也定位于9p24.3。我们发现,XY女性中DMRT1编码区和DMRT2的DM结构域中的点突变并不常见。我们通过荧光原位杂交分析表明,在报道的最小的导致性反转的9p缺失中,这两个基因均被删除,这表明9p缺失个体的性腺发育不全可能是由于DMRT1和DMRT2的联合半合子性所致。

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