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利用高通量测量技术鉴定转录和表观遗传调控因子的作用原则。

Using High-Throughput Measurements to Identify Principles of Transcriptional and Epigenetic Regulators.

机构信息

Biophysics Program, Stanford University, Stanford, CA, USA.

Bioengineering Department, Stanford University, Stanford, CA, USA.

出版信息

Methods Mol Biol. 2024;2842:79-101. doi: 10.1007/978-1-0716-4051-7_4.

Abstract

To achieve exquisite control over the epigenome, we need a better predictive understanding of how transcription factors, chromatin regulators, and their individual domain's function, both as modular parts and as full proteins. Transcriptional effector domains are one class of protein domains that regulate transcription and chromatin. These effector domains either repress or activate gene expression by interacting with chromatin-modifying enzymes, transcriptional cofactors, and/or general transcriptional machinery. Here, we discuss important design considerations for high-throughput investigations of effector domains, recent advances in discovering new domains in human cells and testing how domain function depends on amino acid sequence. For every effector domain, we would like to know the following: What role does the cell type, signaling state, and targeted context have on activation, silencing, and epigenetic memory? Large-scale measurements of transcriptional activities can help systematically answer these questions and identify general rules for how all these parameters affect effector domain activities. Last, we discuss what steps need to be taken to turn a newly discovered effector domain into a robust, precise epigenome editor. With more carefully considered high-throughput investigations, soon we will have better predictive control over the epigenome.

摘要

为了实现对表观基因组的精确控制,我们需要更好地预测转录因子、染色质调节剂及其单个结构域的功能,包括作为模块化部分和完整蛋白质的功能。转录效应结构域是一类调节转录和染色质的蛋白质结构域。这些效应结构域通过与染色质修饰酶、转录共因子和/或一般转录机制相互作用,抑制或激活基因表达。在这里,我们讨论了高通量研究效应结构域的重要设计考虑因素,以及在人类细胞中发现新结构域和测试结构域功能如何依赖于氨基酸序列方面的最新进展。对于每个效应结构域,我们都想知道以下几点:细胞类型、信号状态和靶向背景如何影响激活、沉默和表观遗传记忆?大规模的转录活性测量可以帮助系统地回答这些问题,并确定所有这些参数如何影响效应结构域活性的一般规则。最后,我们讨论了需要采取哪些步骤将新发现的效应结构域转化为稳健、精确的表观基因组编辑器。通过更精心考虑的高通量研究,我们很快就能更好地预测和控制表观基因组。

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