CLK-2/TEL2 is a conserved component of the nonsense-mediated mRNA decay pathway.

Nonsense-mediated mRNA decay (NMD) controls eukaryotic mRNA quality, inducing the degradation of faulty transcripts. Key players in the NMD pathway were originally identified, through genetics, in Caenorhabditis elegans as smg (suppressor with morphological effect on genitalia) genes. Using forward...

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Main Authors: Yanwu Guo, Cristina Tocchini, Rafal Ciosk
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0244505
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spelling doaj-01b3553449d844b6ba1df4199cd2e8152021-04-25T04:30:35ZengPublic Library of Science (PLoS)PLoS ONE1932-62032021-01-01161e024450510.1371/journal.pone.0244505CLK-2/TEL2 is a conserved component of the nonsense-mediated mRNA decay pathway.Yanwu GuoCristina TocchiniRafal CioskNonsense-mediated mRNA decay (NMD) controls eukaryotic mRNA quality, inducing the degradation of faulty transcripts. Key players in the NMD pathway were originally identified, through genetics, in Caenorhabditis elegans as smg (suppressor with morphological effect on genitalia) genes. Using forward genetics and fluorescence-based NMD reporters, we reexamined the genetic landscape underlying NMD. Employing a novel strategy for mapping sterile mutations, Het-Map, we identified clk-2, a conserved gene previously implicated in DNA damage signaling, as a player in the nematode NMD. We find that CLK-2 is expressed predominantly in the germline, highlighting the importance of auxiliary factors in tissue-specific mRNA decay. Importantly, the human counterpart of CLK-2/TEL2, TELO2, has been also implicated in the NMD, suggesting a conserved role of CLK-2/TEL2 proteins in mRNA surveillance. Recently, variants of TELO2 have been linked to an intellectual disability disorder, the You-Hoover-Fong syndrome, which could be related to its function in the NMD.https://doi.org/10.1371/journal.pone.0244505
collection DOAJ
language English
format Article
sources DOAJ
author Yanwu Guo
Cristina Tocchini
Rafal Ciosk
spellingShingle Yanwu Guo
Cristina Tocchini
Rafal Ciosk
CLK-2/TEL2 is a conserved component of the nonsense-mediated mRNA decay pathway.
PLoS ONE
author_facet Yanwu Guo
Cristina Tocchini
Rafal Ciosk
author_sort Yanwu Guo
title CLK-2/TEL2 is a conserved component of the nonsense-mediated mRNA decay pathway.
title_short CLK-2/TEL2 is a conserved component of the nonsense-mediated mRNA decay pathway.
title_full CLK-2/TEL2 is a conserved component of the nonsense-mediated mRNA decay pathway.
title_fullStr CLK-2/TEL2 is a conserved component of the nonsense-mediated mRNA decay pathway.
title_full_unstemmed CLK-2/TEL2 is a conserved component of the nonsense-mediated mRNA decay pathway.
title_sort clk-2/tel2 is a conserved component of the nonsense-mediated mrna decay pathway.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2021-01-01
description Nonsense-mediated mRNA decay (NMD) controls eukaryotic mRNA quality, inducing the degradation of faulty transcripts. Key players in the NMD pathway were originally identified, through genetics, in Caenorhabditis elegans as smg (suppressor with morphological effect on genitalia) genes. Using forward genetics and fluorescence-based NMD reporters, we reexamined the genetic landscape underlying NMD. Employing a novel strategy for mapping sterile mutations, Het-Map, we identified clk-2, a conserved gene previously implicated in DNA damage signaling, as a player in the nematode NMD. We find that CLK-2 is expressed predominantly in the germline, highlighting the importance of auxiliary factors in tissue-specific mRNA decay. Importantly, the human counterpart of CLK-2/TEL2, TELO2, has been also implicated in the NMD, suggesting a conserved role of CLK-2/TEL2 proteins in mRNA surveillance. Recently, variants of TELO2 have been linked to an intellectual disability disorder, the You-Hoover-Fong syndrome, which could be related to its function in the NMD.
url https://doi.org/10.1371/journal.pone.0244505
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