Li L L, Zhu Y Z, Yu X W, Wang R X, Hu Z M, Liu R Z
Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital, Jilin University, Changchun, China.
Department of Genetic Biology, Norman Bethune Medical School, Jilin University, Changchun, China.
Genet Mol Res. 2015 Mar 20;14(1):1932-41. doi: 10.4238/2015.March.20.3.
Y chromosome microdeletions can cause male infertility and are classified as natural transmission and de novo mutations. To examine the source of these deletions in Chinese men and to provide a theoretical and laboratory basis for genetic counseling, patients from Northeast China with primary male infertility (N = 22) and their fathers were investigated. Karyotype analysis was performed on peripheral blood lymphocytes using standard G-banding. Multiplex polymerase chain reaction amplification using 18 specific sequence-tagged sites was selected to detect Y chromosome microdeletions. De novo mutations were observed in 17 father-son pairs, leading to a mutation rate of 77.27% (17/22), while the vertical transmission of Yq AZFc microdeletions was detected in 5 cases of the families investigated (29.41%, 5/17). There were no statistically significant differences between vertically transmitted and de novo mutations in men with AZFc deletions regarding age, testicular volume, and reproductive hormone levels. Most Y chromosome microdeletions in men from Northeast China are the result of de novo mutations via natural conception, and men with Yq AZFc deletions showed no clear differences between vertical transmission and de novo mutations.
Y染色体微缺失可导致男性不育,分为自然传递和新发突变。为了研究中国男性中这些缺失的来源,并为遗传咨询提供理论和实验室依据,对来自中国东北的原发性男性不育患者(N = 22)及其父亲进行了调查。使用标准G显带对外周血淋巴细胞进行核型分析。选择使用18个特异性序列标签位点的多重聚合酶链反应扩增来检测Y染色体微缺失。在17对父子对中观察到新发突变,导致突变率为77.27%(17/22),而在所调查的家庭中有5例检测到Yq AZFc微缺失的垂直传递(29.41%,5/17)。在年龄、睾丸体积和生殖激素水平方面,AZFc缺失男性的垂直传递和新发突变之间没有统计学上的显著差异。中国东北男性的大多数Y染色体微缺失是自然受孕过程中新发突变的结果,Yq AZFc缺失的男性在垂直传递和新发突变之间没有明显差异。