Long non-coding RNAs: roles in cellular stress responses and epigenetic mechanisms regulating chromatin

被引:6
作者
Nickerson, Jeffrey A. [1 ]
Momen-Heravi, Fatemeh [2 ,3 ]
机构
[1] Univ Massachusetts, Chan Med Sch, Dept Pediat, Div Genes & Dev, Worcester, MA 01003 USA
[2] Columbia Univ, Med Ctr, Coll Dent Med, New York, NY 10032 USA
[3] Columbia Univ, Herbert Irving Comprehens Canc Ctr, New York, NY USA
关键词
Building RNA structures; chromatin architecture; genome-wide lncRNA screens; lncRNA; RNP networks; stress response; HETEROGENEOUS NUCLEAR-RNA; R-LOOP FORMATION; HNRNP-U/SAF-A; BIOCHEMICAL-CHARACTERIZATION; RIBONUCLEOPROTEIN NETWORK; PHASE-SEPARATION; DNA-REPLICATION; GENE; MALAT1; PROTEIN;
D O I
10.1080/19491034.2024.2350180
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Most of the genome is transcribed into RNA but only 2% of the sequence codes for proteins. Non-coding RNA transcripts include a very large number of long noncoding RNAs (lncRNAs). A growing number of identified lncRNAs operate in cellular stress responses, for example in response to hypoxia, genotoxic stress, and oxidative stress. Additionally, lncRNA plays important roles in epigenetic mechanisms operating at chromatin and in maintaining chromatin architecture. Here, we address three lncRNA topics that have had significant recent advances. The first is an emerging role for many lncRNAs in cellular stress responses. The second is the development of high throughput screening assays to develop causal relationships between lncRNAs across the genome with cellular functions. Finally, we turn to recent advances in understanding the role of lncRNAs in regulating chromatin architecture and epigenetics, advances that build on some of the earliest work linking RNA to chromatin architecture.
引用
收藏
页数:25
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