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APOBEC1 补体因子(A1cf)突变小鼠中的基因偏向性受精。

Genetically-biased fertilization in APOBEC1 complementation factor (A1cf) mutant mice.

机构信息

Institute for Biogenesis Research, John A. Burns School of Medicine, University of Hawaii at Manoa, Honolulu, HI, USA.

Center for Molecular Medicine, Maine Medical Center Research Institute, Portland, ME, USA.

出版信息

Sci Rep. 2022 Aug 10;12(1):13599. doi: 10.1038/s41598-022-17948-9.

Abstract

Meiosis, recombination, and gametogenesis normally ensure that gametes combine randomly. But in exceptional cases, fertilization depends on the genetics of gametes from both females and males. A key question is whether their non-random union results from factors intrinsic to oocytes and sperm, or from their interactions with conditions in the reproductive tracts. To address this question, we used in vitro fertilization (IVF) with a mutant and wild-type allele of the A1cf (APOBEC1 complementation factor) gene in mice that are otherwise genetically identical. We observed strong distortion in favor of mutant heterozygotes showing that bias depends on the genetics of oocyte and sperm, and that any environmental input is modest. To search for the potential mechanism of the 'biased fertilization', we analyzed the existing transcriptome data and demonstrated that localization of A1cf transcripts and its candidate mRNA targets is restricted to the spermatids in which they originate, and that these transcripts are enriched for functions related to meiosis, fertilization, RNA stability, translation, and mitochondria. We propose that failure to sequester mRNA targets in A1cf mutant heterozygotes leads to functional differences among spermatids, thereby providing an opportunity for selection among haploid gametes. The study adds to the understanding of the gamete interaction at fertilization. Discovery that bias is evident with IVF provides a new venue for future explorations of preference among genetically distinct gametes at fertilization for A1cf and other genes that display significant departure of Mendelian inheritance.

摘要

减数分裂、重组和配子发生通常确保配子随机结合。但在特殊情况下,受精取决于来自雌性和雄性配子的遗传学。一个关键问题是,它们的非随机结合是来自卵母细胞和精子的内在因素,还是来自它们与生殖道条件的相互作用。为了解决这个问题,我们使用了在体外受精(IVF)中使用 A1cf(APOBEC1 互补因子)基因的突变体和野生型等位基因的方法,这些基因在其他方面是完全相同的。我们观察到强烈的偏向有利于突变杂合子,表明这种偏向取决于卵母细胞和精子的遗传学,任何环境输入都是适度的。为了寻找“偏向受精”的潜在机制,我们分析了现有的转录组数据,并证明了 A1cf 转录本及其候选 mRNA 靶标定位于它们起源的精原细胞中,这些转录本富集了与减数分裂、受精、RNA 稳定性、翻译和线粒体相关的功能。我们提出,在 A1cf 突变杂合子中未能将 mRNA 靶标隔离会导致精原细胞之间的功能差异,从而为单倍体配子之间的选择提供机会。该研究增加了对受精时配子相互作用的理解。发现 IVF 中的偏向为未来探索 A1cf 和其他显示孟德尔遗传明显偏离的基因在受精时在遗传上不同的配子之间的偏好提供了新的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5437/9365768/8048fa8f52a2/41598_2022_17948_Fig1_HTML.jpg

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