Boucekkine C, Vilain E, McElreavey K, Jaubert F, Brauner R, Thibaud E, Battin J, Toublanc J E, Kucheria K, Chaabouni S
Laboratoire d'Immunogénétique Humaine, Institut Pasteur, Paris.
Ann Endocrinol (Paris). 1994;54(5):315-21.
During mammalian embryogenesis, the presence of the SRY gene determines the bipotential gonad to develop as a testis. 46,XY sex reversal has been described in man. It is associated with an essentially female phenotype and a streak gonad. In a collaborative study, we analysed 36 patients with a 46,XY sex reversal. The testis determining region of the Y chromosome was analysed by Southern blotting and by DGGE analysis of the SRY open reading frame (orf). We found a total of 7 mutations in the testis determining region including the SRY gene. This brings to 19 the total number of mutations in SRY associated with sex reversal. No relationship was found between the SRY status and the presence or absence of gonadoblastoma. However, a correlation was observed between the SRY genotype and the histology of the gonad. A mutant in SRY is associated with a completely dysgenetic gonad. The presence of immature testicular tubules is usually observed when SRY is normal. These latter results suggest the existence of as yet unidentified testis determining genes.
在哺乳动物胚胎发育过程中,SRY基因的存在决定了双潜能性腺发育为睾丸。人类中已描述了46,XY性反转情况。它与基本为女性的表型和条索状性腺相关。在一项合作研究中,我们分析了36例46,XY性反转患者。通过Southern印迹法以及对SRY开放阅读框(orf)进行变性梯度凝胶电泳(DGGE)分析,对Y染色体的睾丸决定区域进行了分析。我们在包括SRY基因在内的睾丸决定区域共发现了7个突变。这使得与性反转相关的SRY突变总数达到了19个。未发现SRY状态与性腺母细胞瘤的有无之间存在关联。然而,观察到SRY基因型与性腺组织学之间存在相关性。SRY中的一个突变与完全发育不全的性腺相关。当SRY正常时,通常会观察到未成熟的睾丸小管。后一结果提示存在尚未鉴定的睾丸决定基因。