Mohandas T K, Speed R M, Passage M B, Yen P H, Chandley A C, Shapiro L J
Division of Medical Genetics, Harbor-UCLA Medical Center, Torrance 90509.
Am J Hum Genet. 1992 Sep;51(3):526-33.
Meiotic studies were undertaken in a 24-year-old male patient with short stature, chondrodysplasia punctata, ichthyosis, steroid sulfatase deficiency, and mild mental retardation with an inherited cytologically visible deletion of distal Xp. Molecular investigations showed that the pseudoautosomal region as well as the steroid sulfatase gene were deleted, but telomeric sequences were present at the pter on the deleted X chromosome. A complete failure of sex-chromosome pairing was observed in the primary spermatocytes of the patient. Telomeric approaches between the sex chromosomes were made at zygotene in some cells, but no XY synaptonemal complex was formed. The sex chromosomes were present as univalents at metaphase I, and germ-cell development was arrested between metaphase I and metaphase II in the vast majority of cells, consistent with the azoospermia observed in the patient. The failure of XY pairing in this individual indicates that the pseudoautosomal sequences play an important role in initiating XY pairing and formation of synaptonemal complex at meiosis.
对一名24岁男性患者进行了减数分裂研究,该患者身材矮小、点状软骨发育不良、鱼鳞病、类固醇硫酸酯酶缺乏症且轻度智力发育迟缓,其遗传性细胞学可见的Xp远端缺失。分子研究表明,假常染色体区域以及类固醇硫酸酯酶基因均被缺失,但在缺失的X染色体的pter处存在端粒序列。在患者的初级精母细胞中观察到性染色体配对完全失败。在一些细胞的偶线期,性染色体之间进行了端粒连接,但未形成XY联会复合体。在中期I,性染色体以单价体形式存在,并且在绝大多数细胞中生殖细胞发育在中期I和中期II之间停滞,这与在患者中观察到的无精子症一致。该个体中XY配对失败表明假常染色体序列在减数分裂时启动XY配对和联会复合体形成中起重要作用。