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Measurement by quantitative PCR of changes in HPRT, PGK-1, PGK-2, APRT, MTase, and Zfy gene transcripts during mouse spermatogenesis

机译:通过定量PCR测量小鼠精子发生过程中HPRT,PGK-1,PGK-2,APRT,MTase和Zfy基因转录本的变化

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摘要

A reverse transcriptase-polymerase chain reaction assay (RT-PCR) was used quantitatively to measure accumulated levels of RNA transcripts in total mouse RNAs derived from male germ cells at various spermatogenic stages. RNA levels for two X-linked enzymes, phosphoglycerate kinase (PGK-1) and hypoxanthine phosphoribosyl transferase (HPRT), both decrease during spermatogenesis, although the transcript levels decrease much more rapidly for PGK-1. RNA for the Y-linked ZFY (zinc finger protein) is elevated in all spermatogenic cell fractions tested, being particularly high in leptotene/zygotene spermatocytes and round spermatids. RNA for adenine phosphoribosyltransferase (APRT) increases 5-fold to a peak during late pachynema. RNA for PGK-2, undetectable in spermatogonial cells, increases at least 50-fold by the round spermatid stage. DNA (cytosine-5-)-methyltransferase (MTase) transcript levels are over an order of magnitude higher throughout spermatogenesis than in non-dividing liver cells.
机译:定量使用逆转录聚合酶链反应(RT-PCR)来测量在各个生精阶段衍生自雄性生殖细胞的小鼠总RNA中RNA转录物的累积水平。两种X连锁酶,磷酸甘油酸激酶(PGK-1)和次黄嘌呤磷酸核糖基转移酶(HPRT)的RNA水平在精子发生过程中均降低,尽管PGK-1的转录水平下降得更快。 Y-连接的ZFY(锌指蛋白)的RNA在所有测试的生精细胞组分中均升高,尤其是在瘦素/合子精子细胞和圆形精子中含量更高。腺嘌呤磷酸核糖基转移酶(APRT)的RNA在早产儿晚期增加5倍至峰值。 PGK-2的RNA在精原细胞中无法检测到,在圆形的精子细胞阶段增加了至少50倍。在整个精子发生过程中,DNA(胞嘧啶-5-)-甲基转移酶(MTase)的转录水平要比不分裂的肝细胞高一个数量级。

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