» Articles » PMID: 24567736

Cytoplasmic 5'-3' Exonuclease Xrn1p is Also a Genome-wide Transcription Factor in Yeast

Overview
Journal Front Genet
Date 2014 Feb 26
PMID 24567736
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

The 5' to 3' exoribonuclease Xrn1 is a large protein involved in cytoplasmatic mRNA degradation as a critical component of the major decaysome. Its deletion in the yeast Saccharomyces cerevisiae is not lethal, but it has multiple physiological effects. In a previous study, our group showed that deletion of all tested components of the yeast major decaysome, including XRN1, results in a decrease in the synthetic rate and an increase in half-life of most mRNAs in a compensatory manner. Furthermore, the same study showed that the all tested decaysome components are also nuclear proteins that bind to the 5' region of a number of genes. In the present work, we show that disruption of Xrn1 activity preferentially affects both the synthesis and decay of a distinct subpopulation of mRNAs. The most affected mRNAs are the transcripts of the highly transcribed genes, mainly those encoding ribosome biogenesis and translation factors. Previously, we proposed that synthegradases play a key role in regulating both mRNA synthesis and degradation. Evidently, Xrn1 functions as a synthegradase, whose selectivity might help coordinating the expression of the protein synthetic machinery. We propose to name the most affected genes "Xrn1 synthegradon."

Citing Articles

The potential of Paraburkholderia species to enhance crop growth.

Rojas-Rojas F, Gomez-Vazquez I, Estrada-de Los Santos P, Shimada-Beltran H, Vega-Arreguin J World J Microbiol Biotechnol. 2025; 41(2):62.

PMID: 39904926 PMC: 11794353. DOI: 10.1007/s11274-025-04256-3.


Proper 5'-3' cotranslational mRNA decay in yeast requires import of Xrn1 to the nucleus.

Jordan-Pla A, Zhang Y, Garcia-Martinez J, Chattopadhyay S, Forte A, Choder M PLoS One. 2025; 20(1):e0308195.

PMID: 39841709 PMC: 11753706. DOI: 10.1371/journal.pone.0308195.


Evolutionary adaptation under climate change: sp. demonstrates potential to adapt to warming.

Couper L, Dodge T, Hemker J, Kim B, Exposito-Alonso M, Brem R Proc Natl Acad Sci U S A. 2025; 122(2):e2418199122.

PMID: 39772738 PMC: 11745351. DOI: 10.1073/pnas.2418199122.


Homeostasis of mRNA concentrations through coupling transcription, export, and degradation.

Wang Q, Lin J iScience. 2024; 27(8):110531.

PMID: 39175768 PMC: 11338957. DOI: 10.1016/j.isci.2024.110531.


Microglia-targeted inhibition of miR-17 via mannose-coated lipid nanoparticles improves pathology and behavior in a mouse model of Alzheimer's disease.

Badr A, Daily K, Eltobgy M, Estfanous S, Tan M, Chun-Tien Kuo J Brain Behav Immun. 2024; 119:919-944.

PMID: 38718909 PMC: 11781315. DOI: 10.1016/j.bbi.2024.05.006.


References
1.
Muhlrad D, Decker C, Parker R . Deadenylation of the unstable mRNA encoded by the yeast MFA2 gene leads to decapping followed by 5'-->3' digestion of the transcript. Genes Dev. 1994; 8(7):855-66. DOI: 10.1101/gad.8.7.855. View

2.
Hieronymus H, Silver P . Genome-wide analysis of RNA-protein interactions illustrates specificity of the mRNA export machinery. Nat Genet. 2003; 33(2):155-61. DOI: 10.1038/ng1080. View

3.
Perez-Ortin J, Alepuz P, Chavez S, Choder M . Eukaryotic mRNA decay: methodologies, pathways, and links to other stages of gene expression. J Mol Biol. 2013; 425(20):3750-75. DOI: 10.1016/j.jmb.2013.02.029. View

4.
Kim J, Kim J . KEM1 is involved in filamentous growth of Saccharomyces cerevisiae. FEMS Microbiol Lett. 2002; 216(1):33-8. DOI: 10.1111/j.1574-6968.2002.tb11410.x. View

5.
Pelechano V, Jimeno-Gonzalez S, Rodriguez-Gil A, Garcia-Martinez J, Perez-Ortin J, Chavez S . Regulon-specific control of transcription elongation across the yeast genome. PLoS Genet. 2009; 5(8):e1000614. PMC: 2721418. DOI: 10.1371/journal.pgen.1000614. View