» Articles » PMID: 30216698

Environmental Influences on RNA Processing: Biochemical, Molecular and Genetic Regulators of Cellular Response

Overview
Publisher Wiley
Date 2018 Sep 15
PMID 30216698
Citations 21
Authors
Affiliations
Soon will be listed here.
Abstract

RNA processing has emerged as a key mechanistic step in the regulation of the cellular response to environmental perturbation. Recent work has uncovered extensive remodeling of transcriptome composition upon environmental perturbation and linked the impacts of this molecular plasticity to health and disease outcomes. These isoform changes and their underlying mechanisms are varied-involving alternative sites of transcription initiation, alternative splicing, and alternative cleavage at the 3' end of the mRNA. The mechanisms and consequences of differential RNA processing have been characterized across a range of common environmental insults, including chemical stimuli, immune stimuli, heat stress, and cancer pathogenesis. In each case, there are perturbation-specific contributions of local (cis) regulatory elements or global (trans) factors and downstream consequences. Overall, it is clear that choices in isoform usage involve a balance between the usage of specific genetic elements (i.e., splice sites, polyadenylation sites) and the timing at which certain decisions are made (i.e., transcription elongation rate). Fine-tuned cellular responses to environmental perturbation are often dependent on the genetic makeup of the cell. Genetic analyses of interindividual variation in splicing have identified genetic effects on splicing that contribute to variation in complex traits. Finally, the increase in the number of tissue types and environmental conditions analyzed for RNA processing is paralleled by the need to develop appropriate analytical tools. The combination of large datasets, novel methods and conditions explored promises to provide a much greater understanding of the role of RNA processing response in human phenotypic variation. This article is categorized under: RNA Processing > RNA Editing and Modification RNA Evolution and Genomics > Computational Analyses of RNA RNA Processing > Splicing Mechanisms RNA Processing > Splicing Regulation/Alternative Splicing.

Citing Articles

A Proposal for the RNAome at the Dawn of the Last Universal Common Ancestor.

Palacios-Perez M, Jose M Genes (Basel). 2024; 15(9).

PMID: 39336786 PMC: 11431127. DOI: 10.3390/genes15091195.


Clinical implications of single cell sequencing for bladder cancer.

Yadollahvandmiandoab R, Jalalizadeh M, Dionato F, Buosi K, Leme P, Col L Oncol Res. 2024; 32(4):597-605.

PMID: 38560564 PMC: 10972735. DOI: 10.32604/or.2024.045442.


mRNA initiation and termination are spatially coordinated.

Calvo-Roitberg E, Carroll C, Venev S, Kim G, Mick S, Dekker J bioRxiv. 2024; .

PMID: 38260419 PMC: 10802295. DOI: 10.1101/2024.01.05.574404.


Evolutionary constraint and innovation across hundreds of placental mammals.

Christmas M, Kaplow I, Genereux D, Dong M, Hughes G, Li X Science. 2023; 380(6643):eabn3943.

PMID: 37104599 PMC: 10250106. DOI: 10.1126/science.abn3943.


Climate change shapes the future evolution of plant metabolism.

Xu S, Weng J Adv Genet (Hoboken). 2023; 1(1):e10022.

PMID: 36619247 PMC: 9744464. DOI: 10.1002/ggn2.10022.


References
1.
Munding E, Shiue L, Katzman S, Donohue J, Ares Jr M . Competition between pre-mRNAs for the splicing machinery drives global regulation of splicing. Mol Cell. 2013; 51(3):338-48. PMC: 3771316. DOI: 10.1016/j.molcel.2013.06.012. View

2.
Dvinge H, Bradley R . Widespread intron retention diversifies most cancer transcriptomes. Genome Med. 2015; 7(1):45. PMC: 4480902. DOI: 10.1186/s13073-015-0168-9. View

3.
Knowles D, Burrows C, Blischak J, Patterson K, Serie D, Norton N . Determining the genetic basis of anthracycline-cardiotoxicity by molecular response QTL mapping in induced cardiomyocytes. Elife. 2018; 7. PMC: 6010343. DOI: 10.7554/eLife.33480. View

4.
Jan C, Friedman R, Ruby J, Bartel D . Formation, regulation and evolution of Caenorhabditis elegans 3'UTRs. Nature. 2010; 469(7328):97-101. PMC: 3057491. DOI: 10.1038/nature09616. View

5.
Nie Z, Hu G, Wei G, Cui K, Yamane A, Resch W . c-Myc is a universal amplifier of expressed genes in lymphocytes and embryonic stem cells. Cell. 2012; 151(1):68-79. PMC: 3471363. DOI: 10.1016/j.cell.2012.08.033. View