Literature DB >> 32816903

Transcriptional adaptation: a mechanism underlying genetic robustness.

Tamar E Sztal1, Didier Y R Stainier2.   

Abstract

Mutations play a crucial role in evolution as they provide the genetic variation that allows evolutionary change. Although some mutations in regulatory elements or coding regions can be beneficial, a large number of them disrupt gene function and reduce fitness. Organisms utilize several mechanisms to compensate for the damaging consequences of genetic perturbations. One such mechanism is the recently identified process of transcriptional adaptation (TA): during this event, mutations that cause mutant mRNA degradation trigger the transcriptional modulation of so-called adapting genes. In some cases, for example when one (or more) of the upregulated genes is functionally redundant with the mutated gene, this process compensates for the loss of the mutated gene's product. Notably, unlike other mechanisms underlying genetic robustness, TA is not triggered by the loss of protein function, an observation that has prompted studies into the machinery of TA and the contexts in which it functions. Here, we review the discovery and current understanding of TA, and discuss how its main features appear to be conserved across species. In light of these findings, we also speculate on the importance of TA in the context of human disease, and provide some recommendations for genome-editing strategies that should be more effective.
© 2020. Published by The Company of Biologists Ltd.

Entities:  

Keywords:  Gene expression; Genetic compensation; Genetic robustness; Genetic variation; Transcriptional adaptation

Mesh:

Substances:

Year:  2020        PMID: 32816903     DOI: 10.1242/dev.186452

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  11 in total

1.  CRISPR/Cas9-Mediated Constitutive Loss of VCP (Valosin-Containing Protein) Impairs Proteostasis and Leads to Defective Striated Muscle Structure and Function In Vivo.

Authors:  Philipp Voisard; Federica Diofano; Amelia A Glazier; Wolfgang Rottbauer; Steffen Just
Journal:  Int J Mol Sci       Date:  2022-06-16       Impact factor: 6.208

2.  Proteolysis of fibrillin-2 microfibrils is essential for normal skeletal development.

Authors:  Timothy J Mead; Daniel R Martin; Lauren W Wang; Stuart A Cain; Cagri Gulec; Elisabeth Cahill; Joseph Mauch; Dieter Reinhardt; Cecilia Lo; Clair Baldock; Suneel S Apte
Journal:  Elife       Date:  2022-05-03       Impact factor: 8.713

3.  Endothelial cell-type-specific molecular requirements for angiogenesis drive fenestrated vessel development in the brain.

Authors:  Sweta Parab; Rachael E Quick; Ryota L Matsuoka
Journal:  Elife       Date:  2021-01-18       Impact factor: 8.140

4.  Redundant functions of the SLC5A transporters Rumpel, Bumpel, and Kumpel in ensheathing glial cells.

Authors:  Kerem Yildirim; Bente Winkler; Nicole Pogodalla; Steffi Mackensen; Marie Baldenius; Luis Garcia; Elke Naffin; Silke Rodrigues; Christian Klämbt
Journal:  Biol Open       Date:  2022-01-18       Impact factor: 2.422

Review 5.  The Genomic Architecture of Hidradenitis Suppurativa-A Systematic Review.

Authors:  Nikolai Paul Pace; Dillon Mintoff; Isabella Borg
Journal:  Front Genet       Date:  2022-03-23       Impact factor: 4.599

6.  Zebrafish models of alx-linked frontonasal dysplasia reveal a role for Alx1 and Alx3 in the anterior segment and vasculature of the developing eye.

Authors:  Baul Yoon; Pan Yeung; Nicholas Santistevan; Lauren E Bluhm; Kenta Kawasaki; Janina Kueper; Richard Dubielzig; Jennifer VanOudenhove; Justin Cotney; Eric C Liao; Yevgenya Grinblat
Journal:  Biol Open       Date:  2022-06-07       Impact factor: 2.643

7.  Comparative Morphological, Metabolic and Transcriptome Analyses in elmo1 -/- , elmo2 -/- , and elmo3 -/- Zebrafish Mutants Identified a Functional Non-Redundancy of the Elmo Proteins.

Authors:  Mike Boger; Katrin Bennewitz; David Philipp Wohlfart; Ingrid Hausser; Carsten Sticht; Gernot Poschet; Jens Kroll
Journal:  Front Cell Dev Biol       Date:  2022-07-08

Review 8.  Genotype to Phenotype: CRISPR Gene Editing Reveals Genetic Compensation as a Mechanism for Phenotypic Disjunction of Morphants and Mutants.

Authors:  Cristy M Salanga; Matthew C Salanga
Journal:  Int J Mol Sci       Date:  2021-03-27       Impact factor: 5.923

9.  MgaSpn is a negative regulator of capsule and phosphorylcholine biosynthesis and influences the virulence of Streptococcus pneumoniae D39.

Authors:  Shengnan Xiao; Weicai Suo; Jinghui Zhang; Xuemei Zhang; Yibing Yin; Xinlin Guo; Yuqiang Zheng
Journal:  Virulence       Date:  2021-12       Impact factor: 5.882

10.  Genetic compensation for cilia defects in cep290 mutants by upregulation of cilia-associated small GTPases.

Authors:  Magdalena Cardenas-Rodriguez; Christina Austin-Tse; Judith G M Bergboer; Elisa Molinari; Yuya Sugano; Ruxandra Bachmann-Gagescu; John A Sayer; Iain A Drummond
Journal:  J Cell Sci       Date:  2021-07-22       Impact factor: 5.285

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.