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支持轴突发育的表观遗传机制的新见解:组蛋白标记和 miRNA。

New insights on epigenetic mechanisms supporting axonal development: histone marks and miRNAs.

机构信息

Centro de Investigación en Medicina Traslacional "Severo R Amuchástegui" (CIMETSA), Instituto Universitario Ciencias Biomédicas Córdoba (IUCBC), Córdoba, Argentina.

Instituto de Investigación Médica Mercedes y Martín Ferreyra (INIMEC-CONICET-UNC), Córdoba, Argentina.

出版信息

FEBS J. 2021 Nov;288(22):6353-6364. doi: 10.1111/febs.15673. Epub 2020 Dec 30.

Abstract

Mechanisms supporting axon growth and the establishment of neuronal polarity have remained largely disconnected from their genetic and epigenetic fundamentals. Recently, post-transcriptional modifications of histones involved in chromatin folding and transcription, and microRNAs controlling translation have emerged as regulators of axonal specification, growth, and guidance. In this article, we review novel evidence supporting the concept that epigenetic mechanisms work at both transcriptional and post-transcriptional levels to shape axons. We also discuss the role of splicing on axonal growth, as one of the most (if not the most) powerful post-transcriptional mechanism to diversify genetic information. Overall, we think exploring the gap between epigenetics and axonal growth raises new questions and perspectives to the development of axons in physiological and pathological contexts.

摘要

支持轴突生长和神经元极性建立的机制在很大程度上与其遗传和表观遗传基础脱节。最近,涉及染色质折叠和转录的组蛋白的转录后修饰以及控制翻译的 microRNAs 已成为轴突特化、生长和导向的调节剂。在本文中,我们回顾了支持这样一种概念的新证据,即表观遗传机制在转录和转录后水平上共同作用以塑造轴突。我们还讨论了剪接在轴突生长中的作用,因为它是(如果不是最强大的话)最多样化遗传信息的转录后机制之一。总的来说,我们认为探索表观遗传学和轴突生长之间的差距为生理和病理环境中轴突的发育提出了新的问题和视角。

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