Suppr超能文献

DNMT3L 是 X 染色体紧缩和减数后基因转录的调节剂。

DNMT3L is a regulator of X chromosome compaction and post-meiotic gene transcription.

机构信息

The Department of Anatomy and Developmental Biology, Monash University, Victoria, Australia.

出版信息

PLoS One. 2011 Mar 31;6(3):e18276. doi: 10.1371/journal.pone.0018276.

Abstract

Previous studies on the epigenetic regulator DNA methyltransferase 3-Like (DNMT3L), have demonstrated it is an essential regulator of paternal imprinting and early male meiosis. Dnmt3L is also a paternal effect gene, i.e., wild type offspring of heterozygous mutant sires display abnormal phenotypes suggesting the inheritance of aberrant epigenetic marks on the paternal chromosomes. In order to reveal the mechanisms underlying these paternal effects, we have assessed X chromosome meiotic compaction, XY chromosome aneuploidy rates and global transcription in meiotic and haploid germ cells from male mice heterozygous for Dnmt3L. XY bodies from Dnmt3L heterozygous males were significantly longer than those from wild types, and were associated with a three-fold increase in XY bearing sperm. Loss of a Dnmt3L allele resulted in deregulated expression of a large number of both X-linked and autosomal genes within meiotic cells, but more prominently in haploid germ cells. Data demonstrate that similar to embryonic stem cells, DNMT3L is involved in an auto-regulatory loop in germ cells wherein the loss of a Dnmt3L allele resulted in increased transcription from the remaining wild type allele. In contrast, however, within round spermatids, this auto-regulatory loop incorporated the alternative non-coding alternative transcripts. Consistent with the mRNA data, we have localized DNMT3L within spermatids and sperm and shown that the loss of a Dnmt3L allele results in a decreased DNMT3L content within sperm. These data demonstrate previously unrecognised roles for DNMT3L in late meiosis and in the transcriptional regulation of meiotic and post-meiotic germ cells. These data provide a potential mechanism for some cases of human Klinefelter's and Turner's syndromes.

摘要

先前的研究表明,表观遗传调控因子 DNA 甲基转移酶 3 样(DNMT3L)是父源印记和早期雄性减数分裂的重要调控因子。Dnmt3L 也是一个父本效应基因,即杂合突变半合子雄鼠的野生型后代表现出异常表型,提示父本染色体上存在异常的表观遗传标记遗传。为了揭示这些父本效应的机制,我们评估了 X 染色体减数分裂浓缩、XY 染色体非整倍体率以及减数分裂和单倍体生殖细胞中的全局转录,这些细胞来自 Dnmt3L 杂合子雄性小鼠。与野生型相比,Dnmt3L 杂合子雄性的 XY 体明显更长,并且携带 XY 的精子增加了三倍。Dnmt3L 等位基因的缺失导致减数分裂细胞中大量 X 连锁和常染色体基因的表达失调,但在单倍体生殖细胞中更为明显。数据表明,与胚胎干细胞类似,DNMT3L 参与生殖细胞中的自我调节环,其中 Dnmt3L 等位基因的缺失导致剩余野生型等位基因的转录增加。然而,在圆形精子细胞中,这种自我调节环纳入了替代的非编码替代转录本。与 mRNA 数据一致,我们在精细胞和精子中定位了 DNMT3L,并表明 Dnmt3L 等位基因的缺失导致精子中 DNMT3L 含量降低。这些数据表明 DNMT3L 在晚期减数分裂和减数分裂和减数分裂后生殖细胞的转录调控中具有以前未被认识到的作用。这些数据为人类 Klinefelter 和 Turner 综合征的一些病例提供了潜在的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f57c/3069080/a198afb49e55/pone.0018276.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验