Identification of Chromosome Sequence Motifs That Mediate Meiotic Pairing and Synapsis in C. elegans

C. elegans chromosomes contain specialized regions called pairing centers (PCs) that mediate homologous pairing and synapsis during meiosis. Four related proteins, ZIM-1, -2, -3, and HIM-8, associate with these sites and are required for their essential functions. Here we show that short sequence el...

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Main Authors: Phillips, Carolyn M., Meng, Xiangdong, Zhang, Lei, Chretien, Jacqueline H., Urnov, Fyodor D., Dernburg, Abby F.
Format: Online
Language:English
Published: 2009
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4001799/
id pubmed-4001799
recordtype oai_dc
spelling pubmed-40017992014-04-28 Identification of Chromosome Sequence Motifs That Mediate Meiotic Pairing and Synapsis in C. elegans Phillips, Carolyn M. Meng, Xiangdong Zhang, Lei Chretien, Jacqueline H. Urnov, Fyodor D. Dernburg, Abby F. Article C. elegans chromosomes contain specialized regions called pairing centers (PCs) that mediate homologous pairing and synapsis during meiosis. Four related proteins, ZIM-1, -2, -3, and HIM-8, associate with these sites and are required for their essential functions. Here we show that short sequence elements enriched in the corresponding chromosome regions selectively recruit these proteins in vivo. In vitro analysis using SELEX indicates that each protein’s binding specificity arises from a combination of two zinc fingers and an adjacent domain. Insertion of a cluster of recruiting motifs into a chromosome lacking its endogenous PC is sufficient to restore homologous pairing, synapsis, crossover recombination, and segregation. These findings help to illuminate how chromosome sites mediate essential aspects of meiotic chromosome dynamics. 2009-07-20 2009-08 /pmc/articles/PMC4001799/ /pubmed/19620970 http://dx.doi.org/10.1038/ncb1904 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Phillips, Carolyn M.
Meng, Xiangdong
Zhang, Lei
Chretien, Jacqueline H.
Urnov, Fyodor D.
Dernburg, Abby F.
spellingShingle Phillips, Carolyn M.
Meng, Xiangdong
Zhang, Lei
Chretien, Jacqueline H.
Urnov, Fyodor D.
Dernburg, Abby F.
Identification of Chromosome Sequence Motifs That Mediate Meiotic Pairing and Synapsis in C. elegans
author_facet Phillips, Carolyn M.
Meng, Xiangdong
Zhang, Lei
Chretien, Jacqueline H.
Urnov, Fyodor D.
Dernburg, Abby F.
author_sort Phillips, Carolyn M.
title Identification of Chromosome Sequence Motifs That Mediate Meiotic Pairing and Synapsis in C. elegans
title_short Identification of Chromosome Sequence Motifs That Mediate Meiotic Pairing and Synapsis in C. elegans
title_full Identification of Chromosome Sequence Motifs That Mediate Meiotic Pairing and Synapsis in C. elegans
title_fullStr Identification of Chromosome Sequence Motifs That Mediate Meiotic Pairing and Synapsis in C. elegans
title_full_unstemmed Identification of Chromosome Sequence Motifs That Mediate Meiotic Pairing and Synapsis in C. elegans
title_sort identification of chromosome sequence motifs that mediate meiotic pairing and synapsis in c. elegans
description C. elegans chromosomes contain specialized regions called pairing centers (PCs) that mediate homologous pairing and synapsis during meiosis. Four related proteins, ZIM-1, -2, -3, and HIM-8, associate with these sites and are required for their essential functions. Here we show that short sequence elements enriched in the corresponding chromosome regions selectively recruit these proteins in vivo. In vitro analysis using SELEX indicates that each protein’s binding specificity arises from a combination of two zinc fingers and an adjacent domain. Insertion of a cluster of recruiting motifs into a chromosome lacking its endogenous PC is sufficient to restore homologous pairing, synapsis, crossover recombination, and segregation. These findings help to illuminate how chromosome sites mediate essential aspects of meiotic chromosome dynamics.
publishDate 2009
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4001799/
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