LIN-42, the Caenorhabditis elegans PERIOD homolog, negatively regulates microRNA transcription.

During C. elegans development, microRNAs (miRNAs) function as molecular switches that define temporal gene expression and cell lineage patterns in a dosage-dependent manner. It is critical, therefore, that the expression of miRNAs be tightly regulated so that target mRNA expression is properly contr...

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Main Authors: Roberto Perales, Dana M King, Cristina Aguirre-Chen, Christopher M Hammell
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-07-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC4102445?pdf=render
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author Roberto Perales
Dana M King
Cristina Aguirre-Chen
Christopher M Hammell
author_facet Roberto Perales
Dana M King
Cristina Aguirre-Chen
Christopher M Hammell
author_sort Roberto Perales
collection DOAJ
description During C. elegans development, microRNAs (miRNAs) function as molecular switches that define temporal gene expression and cell lineage patterns in a dosage-dependent manner. It is critical, therefore, that the expression of miRNAs be tightly regulated so that target mRNA expression is properly controlled. The molecular mechanisms that function to optimize or control miRNA levels during development are unknown. Here we find that mutations in lin-42, the C. elegans homolog of the circadian-related period gene, suppress multiple dosage-dependent miRNA phenotypes including those involved in developmental timing and neuronal cell fate determination. Analysis of mature miRNA levels in lin-42 mutants indicates that lin-42 functions to attenuate miRNA expression. Through the analysis of transcriptional reporters, we show that the upstream cis-acting regulatory regions of several miRNA genes are sufficient to promote highly dynamic transcription that is coupled to the molting cycles of post-embryonic development. Immunoprecipitation of LIN-42 complexes indicates that LIN-42 binds the putative cis-regulatory regions of both non-coding and protein-coding genes and likely plays a role in regulating their transcription. Consistent with this hypothesis, analysis of miRNA transcriptional reporters in lin-42 mutants indicates that lin-42 regulates miRNA transcription. Surprisingly, strong loss-of-function mutations in lin-42 do not abolish the oscillatory expression patterns of lin-4 and let-7 transcription but lead to increased expression of these genes. We propose that lin-42 functions to negatively regulate the transcriptional output of multiple miRNAs and mRNAs and therefore coordinates the expression levels of genes that dictate temporal cell fate with other regulatory programs that promote rhythmic gene expression.
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spelling doaj.art-88f1abd464c643fa8da8404d0f32e3802022-12-22T03:09:49ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042014-07-01107e100448610.1371/journal.pgen.1004486LIN-42, the Caenorhabditis elegans PERIOD homolog, negatively regulates microRNA transcription.Roberto PeralesDana M KingCristina Aguirre-ChenChristopher M HammellDuring C. elegans development, microRNAs (miRNAs) function as molecular switches that define temporal gene expression and cell lineage patterns in a dosage-dependent manner. It is critical, therefore, that the expression of miRNAs be tightly regulated so that target mRNA expression is properly controlled. The molecular mechanisms that function to optimize or control miRNA levels during development are unknown. Here we find that mutations in lin-42, the C. elegans homolog of the circadian-related period gene, suppress multiple dosage-dependent miRNA phenotypes including those involved in developmental timing and neuronal cell fate determination. Analysis of mature miRNA levels in lin-42 mutants indicates that lin-42 functions to attenuate miRNA expression. Through the analysis of transcriptional reporters, we show that the upstream cis-acting regulatory regions of several miRNA genes are sufficient to promote highly dynamic transcription that is coupled to the molting cycles of post-embryonic development. Immunoprecipitation of LIN-42 complexes indicates that LIN-42 binds the putative cis-regulatory regions of both non-coding and protein-coding genes and likely plays a role in regulating their transcription. Consistent with this hypothesis, analysis of miRNA transcriptional reporters in lin-42 mutants indicates that lin-42 regulates miRNA transcription. Surprisingly, strong loss-of-function mutations in lin-42 do not abolish the oscillatory expression patterns of lin-4 and let-7 transcription but lead to increased expression of these genes. We propose that lin-42 functions to negatively regulate the transcriptional output of multiple miRNAs and mRNAs and therefore coordinates the expression levels of genes that dictate temporal cell fate with other regulatory programs that promote rhythmic gene expression.http://europepmc.org/articles/PMC4102445?pdf=render
spellingShingle Roberto Perales
Dana M King
Cristina Aguirre-Chen
Christopher M Hammell
LIN-42, the Caenorhabditis elegans PERIOD homolog, negatively regulates microRNA transcription.
PLoS Genetics
title LIN-42, the Caenorhabditis elegans PERIOD homolog, negatively regulates microRNA transcription.
title_full LIN-42, the Caenorhabditis elegans PERIOD homolog, negatively regulates microRNA transcription.
title_fullStr LIN-42, the Caenorhabditis elegans PERIOD homolog, negatively regulates microRNA transcription.
title_full_unstemmed LIN-42, the Caenorhabditis elegans PERIOD homolog, negatively regulates microRNA transcription.
title_short LIN-42, the Caenorhabditis elegans PERIOD homolog, negatively regulates microRNA transcription.
title_sort lin 42 the caenorhabditis elegans period homolog negatively regulates microrna transcription
url http://europepmc.org/articles/PMC4102445?pdf=render
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