Kierszenbaum A L, Tres L L
J Cell Biol. 1975 May;65(2):258-70. doi: 10.1083/jcb.65.2.258.
A whole-mount electron microscope technique has allowed direct visualization of the transcription process in mouse spermatids. Thes observations have been supported by light and electron microscope autoradiographic techniques that employ [3H]uridine and [3H]arginine in attempts to clarify mechanisms of RNA synthesis and their relationship to nuclear histone changes throughout spermiogenesis. Early spermatid genomes are dispersed almost completely, whereas in later spermiogenic steps the posterior or flagellar nuclear region is readily dispersed and the anterior or subacrosomal nuclear region remains compact. Display of genome segments permits identification of regions where transcription complexes, presumably heterogeneous nuclear RNA species, are seen related to chromatin. These complexes appear as ribonucleoprotein chains, some of them of considerable length, decreasing progressively in number in late spermiogenic steps. This decrease coincides with diminishing rates of [3H]uridine incorporation. Two distinct patterns of chromatin have been identified: a beaded chromatin type associated with transcription complexes encounterd in early spermatids; and a smooth chromatin type not involved in transcriptive activity observed in advanced spermiogenic genomes. Protein particles staining densely with phosphotungstic acid become apparent in nuclei of spermatids after [3H]arginine incorporation becomes significant. There is no structural or autoradiographic evidence for the presence of nucleoli during spermiogenesis. From these data and from previous experimental findings, we conclude that: (a) spermatogonia, spermatocytes and Sertoli cells are transcriptionally expressed into heterogeneous nuclear RNA and preribosomal RNA species whereas transcription in spermatids is predominantly heterogeneous nuclear RNA; and (b) the modification of the chromatin patterns in late spermiogenic steps indicates a stabilized genome that restricts transcriptive functions.
一种整装电子显微镜技术使人们能够直接观察小鼠精子细胞中的转录过程。这些观察结果得到了光镜和电镜放射自显影技术的支持,这些技术使用[3H]尿苷和[3H]精氨酸来试图阐明整个精子发生过程中RNA合成的机制及其与核组蛋白变化的关系。早期精子细胞的基因组几乎完全分散,而在精子发生的后期步骤中,后部或鞭毛核区域很容易分散,前部或顶体下核区域则保持紧密。基因组片段的展示允许识别与染色质相关的转录复合体(可能是不均一核RNA种类)所在的区域。这些复合体表现为核糖核蛋白链,其中一些相当长,在精子发生后期数量逐渐减少。这种减少与[3H]尿苷掺入率的降低相吻合。已经鉴定出两种不同的染色质模式:一种是在早期精子细胞中与转录复合体相关的串珠状染色质类型;另一种是在晚期精子发生基因组中观察到的不参与转录活性的光滑染色质类型。在用[3H]精氨酸掺入变得显著后,用磷钨酸染色浓密的蛋白质颗粒在精子细胞核中变得明显。在精子发生过程中没有核仁存在的结构或放射自显影证据。根据这些数据和先前的实验结果,我们得出以下结论:(a)精原细胞、精母细胞和支持细胞转录表达为不均一核RNA和前核糖体RNA种类,而精子细胞中的转录主要是不均一核RNA;(b)精子发生后期染色质模式的改变表明基因组稳定,限制了转录功能。