Osadchuk L V, Vasiliev G V, Ivanov M K, Prasolova M A, Kleshchev M A, Osadchuk A V
Institute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.
Joint Stock Company Vector Best, Novosibirsk region, Russia.
Vavilovskii Zhurnal Genet Selektsii. 2024 Nov;28(7):780-791. doi: 10.18699/vjgb-24-86.
The Y chromosome contains a set of genes with testis-specific expression that are responsible for the development of testes and spermatogenesis, and it is the most important target in the search for genetic causes of male infertility. Most of these genes are located in the "azoospermia factor" AZF locus (regions AZFa, AZFb, and AZFc) on the long arm of the Y chromosome. Microdeletions of the Y chromosome, leading to the removal of the entire AZF locus as well as one or more regions (complete deletions), are one of the leading causes of spermatogenesis impairment and infertility. However, the role of partial AZFc deletions (gr/gr, b2/b3, b1/b3) in spermatogenesis failure is unclear, and their impact on spermatogenesis varies between populations. The aim of the present study was to assess the frequency of various types of AZFc microdeletions and to search for associations with spermatogenesis parameters in men of Slavic ethnicity from the general Russian population (n = 700, average age 25.8 years). To identify AZF microdeletions, the presence/absence of 15 STS markers was analyzed using multiplex real-time polymerase chain reaction. Age, weight, height, and the volume, concentration, total count, proportion of motile and morphologically normal spermatozoa in the ejaculate were recorded for all participants. In the studied sample, 19.9 % (139/700) of men were found to have AZFc microdeletions, of which 16.7 % (117/700) were carriers of a partial b2/b3 deletion, 3.0 % (21/700) had a partial gr/gr deletion, and 0.14 % (1/700) had a complete b2/b4 deletion. Neither AZFa nor AZFb microdeletions nor other types of AZF deletions were detected. The overall frequency of all types of AZFc deletions, as well as each type of partial microdeletion, b2/ b3 and gr/gr, did not differ in the groups of azoospermia, severe oligozoospermia (≤5.0 mill/ml), oligozoospermia (5.0 < SC <16.0 mill/ml), and normal sperm concentration (≥16.0 mill/ml). Comparison of semen parameters in groups with different types of partial AZFc deletions and the control group (without deletions) also did not reveal significant differences. Thus, partial AZFc microdeletions b2/b3 and gr/gr do not have a significant impact on spermatogenesis in Slavic men. It is suggested that in Slavs, partial AZFc microdeletions b2/b3 and gr/gr are fixed in Y haplogroups N3 and R1a, respectively, and their negative impact on spermatogenesis is balanced by other genetic factors. The higher frequency of partial AZFc deletions (19.7 %) in Slavs compared to European populations (7.3 %) established in our study may be explained by the widespread distribution of these Y haplogroups in the Slavic population of Russia.
Y染色体包含一组具有睾丸特异性表达的基因,这些基因负责睾丸的发育和精子发生,是寻找男性不育遗传原因的最重要靶点。这些基因大多位于Y染色体长臂上的“无精子症因子”AZF位点(AZFa、AZFb和AZFc区域)。Y染色体微缺失会导致整个AZF位点以及一个或多个区域被去除(完全缺失),这是精子发生受损和不育的主要原因之一。然而,AZFc部分缺失(gr/gr、b2/b3、b1/b3)在精子发生失败中的作用尚不清楚,其对精子发生的影响因人群而异。本研究的目的是评估俄罗斯普通人群中斯拉夫族男性(n = 700,平均年龄25.8岁)各种类型AZFc微缺失的频率,并寻找与精子发生参数的关联。为了鉴定AZF微缺失,使用多重实时聚合酶链反应分析了15个STS标记的存在与否。记录了所有参与者的年龄、体重、身高以及精液中精子的体积、浓度、总数、活动精子比例和形态正常精子比例。在研究样本中,发现19.9%(139/700)的男性存在AZFc微缺失,其中16.7%(117/700)是b2/b3部分缺失的携带者,3.0%(21/700)有gr/gr部分缺失,0.14%(1/700)有b2/b4完全缺失。未检测到AZFa或AZFb微缺失以及其他类型的AZF缺失。在无精子症、严重少精子症(≤5.0百万/ml)、少精子症(5.0 < SC < 16.0百万/ml)和精子浓度正常(≥16.0百万/ml)的组中,所有类型AZFc缺失以及每种类型的部分微缺失b2/b3和gr/gr的总体频率没有差异。不同类型AZFc部分缺失组与对照组(无缺失)精液参数的比较也未发现显著差异。因此,AZFc部分微缺失b2/b3和gr/gr对斯拉夫族男性的精子发生没有显著影响。有人认为,在斯拉夫人中,AZFc部分微缺失b2/b3和gr/gr分别固定在Y单倍群N3和R1a中,它们对精子发生的负面影响被其他遗传因素所平衡。我们的研究发现,斯拉夫人中AZFc部分缺失(19.7%)的频率高于欧洲人群(7.3%),这可能是由于这些Y单倍群在俄罗斯斯拉夫人群中广泛分布所致。