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Loss of the insulator protein CTCF during nematode evolution

BACKGROUND: The zinc finger (ZF) protein CTCF (CCCTC-binding factor) is highly conserved in Drosophila and vertebrates where it has been shown to mediate chromatin insulation at a genomewide level. A mode of genetic regulation that involves insulators and insulator binding proteins to establish inde...

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Autores principales: Heger, Peter, Marin, Birger, Schierenberg, Einhard
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2749850/
https://www.ncbi.nlm.nih.gov/pubmed/19712444
http://dx.doi.org/10.1186/1471-2199-10-84
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author Heger, Peter
Marin, Birger
Schierenberg, Einhard
author_facet Heger, Peter
Marin, Birger
Schierenberg, Einhard
author_sort Heger, Peter
collection PubMed
description BACKGROUND: The zinc finger (ZF) protein CTCF (CCCTC-binding factor) is highly conserved in Drosophila and vertebrates where it has been shown to mediate chromatin insulation at a genomewide level. A mode of genetic regulation that involves insulators and insulator binding proteins to establish independent transcriptional units is currently not known in nematodes including Caenorhabditis elegans. We therefore searched in nematodes for orthologs of proteins that are involved in chromatin insulation. RESULTS: While orthologs for other insulator proteins were absent in all 35 analysed nematode species, we find orthologs of CTCF in a subset of nematodes. As an example for these we cloned the Trichinella spiralis CTCF-like gene and revealed a genomic structure very similar to the Drosophila counterpart. To investigate the pattern of CTCF occurrence in nematodes, we performed phylogenetic analysis with the ZF protein sets of completely sequenced nematodes. We show that three ZF proteins from three basal nematodes cluster together with known CTCF proteins whereas no zinc finger protein of C. elegans and other derived nematodes does so. CONCLUSION: Our findings show that CTCF and possibly chromatin insulation are present in basal nematodes. We suggest that the insulator protein CTCF has been secondarily lost in derived nematodes like C. elegans. We propose a switch in the regulation of gene expression during nematode evolution, from the common vertebrate and insect type involving distantly acting regulatory elements and chromatin insulation to a so far poorly characterised mode present in more derived nematodes. Here, all or some of these components are missing. Instead operons, polycistronic transcriptional units common in derived nematodes, seemingly adopted their function.
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spelling pubmed-27498502009-09-24 Loss of the insulator protein CTCF during nematode evolution Heger, Peter Marin, Birger Schierenberg, Einhard BMC Mol Biol Research Article BACKGROUND: The zinc finger (ZF) protein CTCF (CCCTC-binding factor) is highly conserved in Drosophila and vertebrates where it has been shown to mediate chromatin insulation at a genomewide level. A mode of genetic regulation that involves insulators and insulator binding proteins to establish independent transcriptional units is currently not known in nematodes including Caenorhabditis elegans. We therefore searched in nematodes for orthologs of proteins that are involved in chromatin insulation. RESULTS: While orthologs for other insulator proteins were absent in all 35 analysed nematode species, we find orthologs of CTCF in a subset of nematodes. As an example for these we cloned the Trichinella spiralis CTCF-like gene and revealed a genomic structure very similar to the Drosophila counterpart. To investigate the pattern of CTCF occurrence in nematodes, we performed phylogenetic analysis with the ZF protein sets of completely sequenced nematodes. We show that three ZF proteins from three basal nematodes cluster together with known CTCF proteins whereas no zinc finger protein of C. elegans and other derived nematodes does so. CONCLUSION: Our findings show that CTCF and possibly chromatin insulation are present in basal nematodes. We suggest that the insulator protein CTCF has been secondarily lost in derived nematodes like C. elegans. We propose a switch in the regulation of gene expression during nematode evolution, from the common vertebrate and insect type involving distantly acting regulatory elements and chromatin insulation to a so far poorly characterised mode present in more derived nematodes. Here, all or some of these components are missing. Instead operons, polycistronic transcriptional units common in derived nematodes, seemingly adopted their function. BioMed Central 2009-08-27 /pmc/articles/PMC2749850/ /pubmed/19712444 http://dx.doi.org/10.1186/1471-2199-10-84 Text en Copyright © 2009 Heger et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Heger, Peter
Marin, Birger
Schierenberg, Einhard
Loss of the insulator protein CTCF during nematode evolution
title Loss of the insulator protein CTCF during nematode evolution
title_full Loss of the insulator protein CTCF during nematode evolution
title_fullStr Loss of the insulator protein CTCF during nematode evolution
title_full_unstemmed Loss of the insulator protein CTCF during nematode evolution
title_short Loss of the insulator protein CTCF during nematode evolution
title_sort loss of the insulator protein ctcf during nematode evolution
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2749850/
https://www.ncbi.nlm.nih.gov/pubmed/19712444
http://dx.doi.org/10.1186/1471-2199-10-84
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