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

被引:11
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
相关论文
共 208 条
[1]  
Abe R., 2023, BPB Reports, V6, P226, DOI [10.1248/bpbreports.6.6226, DOI 10.1248/BPBREPORTS.6.6226]
[2]   p53 induces formation of NEAT1 lncRNA-containing paraspeckles that modulate replication stress response and chemosensitivity [J].
Adriaens, Carmen ;
Standaert, Laura ;
Barra, Jasmine ;
latil, MathilDe ;
Verfaillie, Annelien ;
Kalev, Peter ;
Boeckx, Bram ;
Wijnhoven, Paul W. G. ;
Radaelli, Enrico ;
Vermi, William ;
Leucci, Eleonora ;
Lapouge, Gaelle ;
Beck, Benjamin ;
van den Oord, Joost ;
Nakagawa, Shinichi ;
Hirose, Tetsuro ;
Sablina, Anna A. ;
Lambrechts, Diether ;
Aerts, Stein ;
Blanpain, Cedric ;
Marine, Jean-Christophe .
NATURE MEDICINE, 2016, 22 (08) :861-+
[3]   R-Loop Mediated trans Action of the APOLO Long Noncoding RNA [J].
Ariel, Federico ;
Lucero, Leandro ;
Christ, Aurelie ;
Mammarella, Maria Florencia ;
Jegu, Teddy ;
Veluchamy, Alaguraj ;
Mariappan, Kiruthiga ;
Latrasse, David ;
Blein, Thomas ;
Liu, Chang ;
Benhamed, Moussa ;
Crespi, Martin .
MOLECULAR CELL, 2020, 77 (05) :1055-+
[4]   MALAT1 Long Non-Coding RNA: Functional Implications [J].
Arun, Gayatri ;
Aggarwal, Disha ;
Spector, David L. .
NON-CODING RNA, 2020, 6 (02)
[5]   Differentiation of mammary tumors and reduction in metastasis upon Malat1 lncRNA loss [J].
Arun, Gayatri ;
Diermeier, Sarah ;
Akerman, Martin ;
Chang, Kung-Chi ;
Wilkinson, J. Erby ;
Hearn, Stephen ;
Kim, Youngsoo ;
MacLeod, A. Robert ;
Krainer, Adrian R. ;
Norton, Larry ;
Brogi, Edi ;
Egeblad, Mikala ;
Spector, David L. .
GENES & DEVELOPMENT, 2016, 30 (01) :34-51
[6]   The evolving role of long noncoding RNA HIF1A-AS2 in diabetic retinopathy: a cross-link axis between hypoxia, oxidative stress and angiogenesis via MAPK/VEGF-dependent pathway [J].
Atef, Marwa Mohamed ;
Shafik, Noha M. ;
Hafez, Yasser Mostafa ;
Watany, Mona Mohamed ;
Selim, Amal ;
Shafik, Heba M. ;
El-Deeb, Omnia Safwat .
REDOX REPORT, 2022, 27 (01) :70-78
[7]   Disease-Causing Mutations and Rearrangements in Long Non-coding RNA Gene Loci [J].
Aznaourova, Marina ;
Schmerer, Nils ;
Schmeck, Bernd ;
Schulte, Leon N. .
FRONTIERS IN GENETICS, 2020, 11
[8]   ULTRASTRUCTURAL ORGANIZATION AND BIOCHEMICAL CHARACTERIZATION OF CHROMATIN-RNA-PROTEIN COMPLEXES ISOLATED FROM MAMMALIAN-CELL NUCLEI [J].
BACHELLERIE, JP ;
PUVION, E ;
ZALTA, JP .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1975, 58 (02) :327-337
[9]   Systematic mapping of nuclear domain-associated transcripts reveals speckles and lamina as hubs of functionally distinct retained introns [J].
Barutcu, A. Rasim ;
Wu, Mingkun ;
Braunschweig, Ulrich ;
Dyakov, Boris J. A. ;
Luo, Zheng ;
Turner, Kyle M. ;
Durbic, Tanja ;
Zhen-Yuan Lin ;
Weatheritt, Robert J. ;
Maass, Philipp G. ;
Gingras, Anne-Claude ;
Blencowe, Benjamin J. .
MOLECULAR CELL, 2022, 82 (05) :1035-+
[10]   Differential contribution of steady-state RNA and active transcription in chromatin organization [J].
Barutcu, A. Rasim ;
Blencowe, Benjamin J. ;
Rinn, John L. .
EMBO REPORTS, 2019, 20 (10)