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人类精子发生过程中的染色质重塑起始。

Chromatin remodelling initiation during human spermiogenesis.

机构信息

Department of Obstetrics and Gynaecology, Radboud University Nijmegen Medical Centre , P.O. Box 9101, 6500 HB Nijmegen , Netherlands.

出版信息

Biol Open. 2012 May 15;1(5):446-57. doi: 10.1242/bio.2012844. Epub 2012 Mar 21.

DOI:10.1242/bio.2012844
PMID:23213436
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3507207/
Abstract

During the last phase of spermatogenesis, spermiogenesis, haploid round spermatids metamorphose towards spermatozoa. Extensive cytoplasmic reduction and chromatin remodelling together allow a dramatic decrease of cellular, notably nuclear volume. DNA packing by a nucleosome based chromatin structure is largely replaced by a protamine based one. At the cytoplasmic level among others the acrosome and perinuclear theca (PNT) are formed. In this study we describe the onset of chromatin remodelling to occur concomitantly with acrosome and PNT development. In spread human round spermatid nuclei, we show development of a DAPI-intense doughnut-like structure co-localizing with the acrosomal sac and sub acrosomal PNT. At this structure we observe the first gradual decrease of nucleosomes and several histones. Histone post-translational modifications linked to chromatin remodelling such as H4K8ac and H4K16ac also delineate the doughnut, that is furthermore marked by H3K9me2. During the capping phase of acrosome development, the size of the doughnut-like chromatin domain increases, and this area often is marked by uniform nucleosome loss and the first appearance of transition protein 2 and protamine 1. In the acrosome phase at nuclear elongation, chromatin remodelling follows the downward movement of the marginal ring of the acrosome. Our results indicate that acrosome development and chromatin remodelling are interacting processes. In the discussion we relate chromatin remodelling to the available data on the nuclear envelope and the linker of nucleoskeleton and cytoskeleton (LINC) complex of spermatids, suggesting a signalling route for triggering chromatin remodelling.

摘要

在精子发生的最后阶段,精子变形,单倍体圆形精子细胞向精子转化。广泛的细胞质减少和染色质重塑共同导致细胞,尤其是核体积的显著减少。基于核小体的染色质结构的 DNA 包装在很大程度上被基于鱼精蛋白的结构所取代。在细胞质水平上,除其他外,顶体和核周质(PNT)形成。在本研究中,我们描述了染色质重塑与顶体和 PNT 发育同时发生的起始。在展开的人类圆形精子细胞核中,我们显示出 DAPI 强烈的甜甜圈状结构的发育与顶体囊和亚顶体 PNT 共定位。在这个结构上,我们观察到核小体的第一次逐渐减少和几种组蛋白。与染色质重塑相关的组蛋白翻译后修饰,如 H4K8ac 和 H4K16ac,也勾勒出甜甜圈,该甜甜圈进一步被 H3K9me2 标记。在顶体发育的盖层阶段,甜甜圈状染色质域的大小增加,该区域通常标记为核小体均匀缺失,以及过渡蛋白 2 和鱼精蛋白 1 的首次出现。在核伸长的顶体阶段,染色质重塑遵循顶体边缘环的向下运动。我们的结果表明,顶体发育和染色质重塑是相互作用的过程。在讨论中,我们将染色质重塑与核膜和核骨架和细胞骨架连接体(LINC)复合体的精子的可用数据相关联,提出了触发染色质重塑的信号通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/620d5a07d002/bio-01-05-446-f08.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/208f943e10db/bio-01-05-446-f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/7ae53f328f3d/bio-01-05-446-f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/1dcf080c3ae2/bio-01-05-446-f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/99083d00c035/bio-01-05-446-f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/aea17937d187/bio-01-05-446-f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/e578da44c2bc/bio-01-05-446-f06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/7606e7146a2d/bio-01-05-446-f07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/620d5a07d002/bio-01-05-446-f08.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/208f943e10db/bio-01-05-446-f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/7ae53f328f3d/bio-01-05-446-f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/1dcf080c3ae2/bio-01-05-446-f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/99083d00c035/bio-01-05-446-f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/aea17937d187/bio-01-05-446-f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/e578da44c2bc/bio-01-05-446-f06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/7606e7146a2d/bio-01-05-446-f07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26a3/3507207/620d5a07d002/bio-01-05-446-f08.jpg

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