Post-transcriptional regulatory mechanisms of dosage compensation in vertebrates.

IF 2.1
Nicholas C Lister, Kim L McIntyre, Paul D Waters
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Abstract

Sex chromosome dosage compensation is thought to be essential in species with heteromorphic sex chromosomes. There has been a large emphasis on transcriptional regulation as the primary mechanism restoring gene dosage balance. However, emerging evidence across vertebrate lineages indicates that post-transcriptional mechanisms make critical contributions to balancing X/Z gene dosage in the proteome. Here, we propose potential mechanisms that may be responsible for this post-transcriptional regulation, including nonsense mediated decay (NMD), N6-methyladenosine RNA methylation (m6A) and sex specific micro-RNAs (miRNAs). We propose that multi-layered regulation of sex chromosome dosage is an ancient and widespread strategy. Recognizing the role of post-transcriptional processes not only reframes current models of dosage compensation, but also uncovers novel mechanisms underpinning development, reproduction and disease.

观点:脊椎动物剂量补偿的转录后调控机制。
性染色体剂量补偿被认为在具有异型性染色体的物种中是必要的。人们一直强调转录调控是恢复基因剂量平衡的主要机制。然而,跨脊椎动物谱系的新证据表明,转录后机制对蛋白质组中X/Z基因剂量的平衡起着关键作用。在这里,我们提出了可能负责这种转录后调控的潜在机制,包括无义介导的衰变(NMD), n6 -甲基腺苷RNA甲基化(m6A)和性别特异性微RNA (miRNAs)。我们认为性染色体剂量的多层调控是一种古老而普遍的策略。认识到转录后过程的作用不仅重塑了目前的剂量补偿模型,而且揭示了支持发育、繁殖和疾病的新机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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