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受精、卵母细胞激活、钙释放与表观遗传重塑:来自癌症模型的经验教训。

Fertilization, Oocyte Activation, Calcium Release and Epigenetic Remodelling: Lessons From Cancer Models.

作者信息

Shafqat Areez, Kashir Junaid, Alsalameh Sulaiman, Alkattan Khaled, Yaqinuddin Ahmed

机构信息

College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.

Department of Comparative Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

出版信息

Front Cell Dev Biol. 2022 Mar 4;10:781953. doi: 10.3389/fcell.2022.781953. eCollection 2022.

DOI:10.3389/fcell.2022.781953
PMID:35309905
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8931327/
Abstract

Oocyte activation deficiency (OAD) is the basis of Total Fertilisation Failure (TFF) and is attributed to mutations in the PLCζ gene-termed male factor infertility. This derives abnormal Ca oscillations and could be the main cause of primary disruptions in the gene expression of Ca-related proteins. Epigenetic mechanisms are universally accepted as key regulators of gene expression. However, epigenetic dysregulations have not been considered as potential mechanisms of oocyte-borne OAD. Herein, we discuss changes in the DNA methylome during oogenesis and embryogenesis. We further highlight key pathways comprising the oocyte Ca toolkit, which could be targets of epigenetic alterations, especially aberrations in DNA methylation. Considering that the vast majority of epigenetic modifications examined during fertilization revolve around alterations in DNA methylation, we aim in this article to associate Ca-specific mechanisms with these alterations. To strengthen this perspective, we bring evidence from cancer research on the intricate link between DNA methylation and Ca signaling as cancer research has examined such questions in a lot more detail. From a therapeutic standpoint, if our hypothesis is proven to be correct, this will explain the cause of TFF in idiopathic cases and will open doors for novel therapeutic targets.

摘要

卵母细胞激活缺陷(OAD)是完全受精失败(TFF)的基础,归因于PLCζ基因突变,即所谓的男性因素不育。这会导致异常的钙振荡,可能是钙相关蛋白基因表达原发性破坏的主要原因。表观遗传机制被普遍认为是基因表达的关键调节因子。然而,表观遗传失调尚未被视为卵源性OAD的潜在机制。在此,我们讨论了卵子发生和胚胎发生过程中DNA甲基化组的变化。我们进一步强调了构成卵母细胞钙工具包的关键途径,这些途径可能是表观遗传改变的靶点,尤其是DNA甲基化异常。鉴于受精过程中检测到的绝大多数表观遗传修饰都围绕着DNA甲基化的改变,我们在本文中旨在将钙特异性机制与这些改变联系起来。为了强化这一观点,我们借鉴了癌症研究中关于DNA甲基化与钙信号之间复杂联系的证据,因为癌症研究已经更详细地研究了此类问题。从治疗角度来看,如果我们的假设被证明是正确的,这将解释特发性病例中TFF的原因,并为新的治疗靶点打开大门。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5faf/8931327/d2facaf21b7b/fcell-10-781953-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5faf/8931327/ae2bc6558237/fcell-10-781953-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5faf/8931327/d2facaf21b7b/fcell-10-781953-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5faf/8931327/ae2bc6558237/fcell-10-781953-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5faf/8931327/d2facaf21b7b/fcell-10-781953-g002.jpg

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