Arruda J T, Bordin B M, Santos P R, Mesquita W E J C, Silva R C P C, Maia M C S, Approbato M S, Florêncio R S, Amaral W N, Rocha Filho M A, Moura K K V O
Núcleo de Pesquisas Replicon, Universidade Católica de Goiás, Goiânia, GO, Brasil.
Genet Mol Res. 2007 Jun 30;6(2):461-9.
Microdeletions in Yq are associated with defects in spermatogenesis, while those in the AZF region are considered critical for germ cell development. We examined microdeletions in the Y chromosomes of patients attended at the Laboratory of Human Reproduction of the Clinical Hospital of the Federal University of Goiás as part of a screening of patients who plan to undergo assisted reproduction. Analysis was made of the AZF region of the Y chromosome in men who had altered spermograms to detect possible microdeletions in Yq. Twenty-three patients with azoospermia and 40 with severe oligozoospermia were analyzed by PCR for the detection of six sequence-tagged sites: sY84 and sY86 for AZFa, sY127 and sY134 for AZFb, and sY254 and sY255 for AZFc. Microdeletions were detected in 28 patients, including 10 azoospermics and 18 severe oligozoospermics. The patients with azoospermia had 43.4% of their microdeletions in the AZFa region, 8.6% in the AZFb region and 17.4% in the AZFc region. In the severe oligozoospermics, 40% were in the AZFa region, 5% in the AZFb region and 5% in the AZFc region. We conclude that microdeletions can be the cause of idiopathic male infertility, supporting conclusions from previous studies.
Yq微缺失与精子发生缺陷相关,而AZF区域的微缺失被认为对生殖细胞发育至关重要。作为对计划接受辅助生殖的患者进行筛查的一部分,我们检测了在戈亚斯联邦大学临床医院人类生殖实验室就诊患者的Y染色体微缺失情况。对精子图谱异常的男性的Y染色体AZF区域进行分析,以检测Yq中可能存在的微缺失。通过聚合酶链反应(PCR)对23例无精子症患者和40例严重少精子症患者进行分析,以检测六个序列标签位点:用于AZFa的sY84和sY86、用于AZFb的sY127和sY134以及用于AZFc的sY254和sY255。在28例患者中检测到微缺失,其中包括10例无精子症患者和18例严重少精子症患者。无精子症患者中,43.4%的微缺失位于AZFa区域,8.6%位于AZFb区域,17.4%位于AZFc区域。在严重少精子症患者中,40%位于AZFa区域,5%位于AZFb区域,5%位于AZFc区域。我们得出结论,微缺失可能是特发性男性不育的原因,这支持了先前研究的结论