TY - JOUR
T1 - Evolution of Transcriptional Repressors Impacts Caenorhabditis Vulval Development
AU - Chamberlin, Helen M.
AU - Jain, Ish M.
AU - Corchado-Sonera, Marcos
AU - Kelley, Leanne H.
AU - Sharanya, Devika
AU - Jama, Abdulrahman
AU - Pabla, Romy
AU - Dawes, Adriana T.
AU - Gupta, Bhagwati P.
AU - Ruvinsky, Ilya
N1 - Funding Information:
We thank Ryan Johnson, Jennifer Patritti-Cram, Ayush Ranawade, Bavithra Thillainathan, Nagagireesh Bojanala, and members of the Sternberg lab (Caltech), in particular Shahla Gharib and Keith Brown, for technical assistance in the early phases of this project. We are grateful to Don Moerman and Mark Edgley for ivph-3(gk3691), and Stephane Flibotte for assistance with genome sequence analysis to identify Cbr-ivp candidate genes. Wen Tang provided comments on a previous draft of the manuscript. Some strains were supplied by the Caenorhabditis Genetics Center, which is funded by the NIH Office of Research Infrastructure programs (P40 OD010440). Some plasmids were provided by Addgene.org. Some work was done with the OSU CCC Genomics Shared Resource, which is funded by the National Cancer Institute (P30 CA016058). We thank Wormbase.org for data and images. M.C.-S. was supported by the CMBP predoctoral training grant from the National Institutes of Health (T32-GM086252) and the Pelotonia Cancer Research Graduate Fellowship. This work was supported by the National Science Foundation (DMS-1361251) and NSERC Discovery (RGPIN-2014-05153) grants. RNAseq data are submitted to GEO (GSE133769).
Publisher Copyright:
© 2020 The Author(s). Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. All rights reserved.
PY - 2020/5/1
Y1 - 2020/5/1
N2 - Comparative genomic sequence analysis has found that the genes for many chromatin-associated proteins are poorly conserved, but the biological consequences of these sequence changes are not understood. Here, we show that four genes identified for an Inappropriate Vulval cell Proliferation (ivp) phenotype in the nematode Caenorhabditis briggsae exhibit distinct functions and genetic interactions when compared with their orthologs in C. elegans. Specifically, we show that the four C. briggsae ivp genes encode the noncanonical histone HTZ-1/H2A.z and three nematode-specific proteins predicted to function in the nucleus. The mutants exhibit ectopic vulval precursor cell proliferation (the multivulva [Muv] phenotype) due to inappropriate expression of the lin-3/EGF gene, and RNAseq analysis suggests a broad role for these ivp genes in transcriptional repression. Importantly, although the C. briggsae phenotypes have parallels with those seen in the C. elegans synMuv system, except for the highly conserved HTZ-1/H2A.z, comparable mutations in C. elegans ivp orthologs do not exhibit synMuv gene interactions or phenotypes. These results demonstrate the evolutionary changes that can underlie conserved biological outputs and argue that proteins critical to repress inappropriate expression from the genome participate in a rapidly evolving functional landscape.
AB - Comparative genomic sequence analysis has found that the genes for many chromatin-associated proteins are poorly conserved, but the biological consequences of these sequence changes are not understood. Here, we show that four genes identified for an Inappropriate Vulval cell Proliferation (ivp) phenotype in the nematode Caenorhabditis briggsae exhibit distinct functions and genetic interactions when compared with their orthologs in C. elegans. Specifically, we show that the four C. briggsae ivp genes encode the noncanonical histone HTZ-1/H2A.z and three nematode-specific proteins predicted to function in the nucleus. The mutants exhibit ectopic vulval precursor cell proliferation (the multivulva [Muv] phenotype) due to inappropriate expression of the lin-3/EGF gene, and RNAseq analysis suggests a broad role for these ivp genes in transcriptional repression. Importantly, although the C. briggsae phenotypes have parallels with those seen in the C. elegans synMuv system, except for the highly conserved HTZ-1/H2A.z, comparable mutations in C. elegans ivp orthologs do not exhibit synMuv gene interactions or phenotypes. These results demonstrate the evolutionary changes that can underlie conserved biological outputs and argue that proteins critical to repress inappropriate expression from the genome participate in a rapidly evolving functional landscape.
KW - chromatin
KW - developmental evolution
KW - developmental system drift
KW - transcriptional repression
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U2 - 10.1093/molbev/msaa009
DO - 10.1093/molbev/msaa009
M3 - Article
C2 - 31960924
AN - SCOPUS:85084101999
SN - 0737-4038
VL - 37
SP - 1350
EP - 1361
JO - Molecular Biology and Evolution
JF - Molecular Biology and Evolution
IS - 5
ER -