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Genome-Wide Identification of Polycomb Target Genes Reveals a Functional Association of Pho with Scm in Bombyx mori

Polycomb group (PcG) proteins are evolutionarily conserved chromatin modifiers and act together in three multimeric complexes, Polycomb repressive complex 1 (PRC1), Polycomb repressive complex 2 (PRC2), and Pleiohomeotic repressive complex (PhoRC), to repress transcription of the target genes. Here,...

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Autores principales: Li, Zhiqing, Cheng, Daojun, Mon, Hiroaki, Tatsuke, Tsuneyuki, Zhu, Li, Xu, Jian, Lee, Jae Man, Xia, Qingyou, Kusakabe, Takahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3317521/
https://www.ncbi.nlm.nih.gov/pubmed/22485166
http://dx.doi.org/10.1371/journal.pone.0034330
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author Li, Zhiqing
Cheng, Daojun
Mon, Hiroaki
Tatsuke, Tsuneyuki
Zhu, Li
Xu, Jian
Lee, Jae Man
Xia, Qingyou
Kusakabe, Takahiro
author_facet Li, Zhiqing
Cheng, Daojun
Mon, Hiroaki
Tatsuke, Tsuneyuki
Zhu, Li
Xu, Jian
Lee, Jae Man
Xia, Qingyou
Kusakabe, Takahiro
author_sort Li, Zhiqing
collection PubMed
description Polycomb group (PcG) proteins are evolutionarily conserved chromatin modifiers and act together in three multimeric complexes, Polycomb repressive complex 1 (PRC1), Polycomb repressive complex 2 (PRC2), and Pleiohomeotic repressive complex (PhoRC), to repress transcription of the target genes. Here, we identified Polycomb target genes in Bombyx mori with holocentric centromere using genome-wide expression screening based on the knockdown of BmSCE, BmESC, BmPHO, or BmSCM gene, which represent the distinct complexes. As a result, the expressions of 29 genes were up-regulated after knocking down 4 PcG genes. Particularly, there is a significant overlap between targets of BmPho (331 out of 524) and BmScm (331 out of 532), and among these, 190 genes function as regulator factors playing important roles in development. We also found that BmPho, as well as BmScm, can interact with other Polycomb components examined in this study. Further detailed analysis revealed that the C-terminus of BmPho containing zinc finger domain is involved in the interaction between BmPho and BmScm. Moreover, the zinc finger domain in BmPho contributes to its inhibitory function and ectopic overexpression of BmScm is able to promote transcriptional repression by Gal4-Pho fusions including BmScm-interacting domain. Loss of BmPho expression causes relocalization of BmScm into the cytoplasm. Collectively, we provide evidence of a functional link between BmPho and BmScm, and propose two Polycomb-related repression mechanisms requiring only BmPho associated with BmScm or a whole set of PcG complexes.
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spelling pubmed-33175212012-04-06 Genome-Wide Identification of Polycomb Target Genes Reveals a Functional Association of Pho with Scm in Bombyx mori Li, Zhiqing Cheng, Daojun Mon, Hiroaki Tatsuke, Tsuneyuki Zhu, Li Xu, Jian Lee, Jae Man Xia, Qingyou Kusakabe, Takahiro PLoS One Research Article Polycomb group (PcG) proteins are evolutionarily conserved chromatin modifiers and act together in three multimeric complexes, Polycomb repressive complex 1 (PRC1), Polycomb repressive complex 2 (PRC2), and Pleiohomeotic repressive complex (PhoRC), to repress transcription of the target genes. Here, we identified Polycomb target genes in Bombyx mori with holocentric centromere using genome-wide expression screening based on the knockdown of BmSCE, BmESC, BmPHO, or BmSCM gene, which represent the distinct complexes. As a result, the expressions of 29 genes were up-regulated after knocking down 4 PcG genes. Particularly, there is a significant overlap between targets of BmPho (331 out of 524) and BmScm (331 out of 532), and among these, 190 genes function as regulator factors playing important roles in development. We also found that BmPho, as well as BmScm, can interact with other Polycomb components examined in this study. Further detailed analysis revealed that the C-terminus of BmPho containing zinc finger domain is involved in the interaction between BmPho and BmScm. Moreover, the zinc finger domain in BmPho contributes to its inhibitory function and ectopic overexpression of BmScm is able to promote transcriptional repression by Gal4-Pho fusions including BmScm-interacting domain. Loss of BmPho expression causes relocalization of BmScm into the cytoplasm. Collectively, we provide evidence of a functional link between BmPho and BmScm, and propose two Polycomb-related repression mechanisms requiring only BmPho associated with BmScm or a whole set of PcG complexes. Public Library of Science 2012-04-02 /pmc/articles/PMC3317521/ /pubmed/22485166 http://dx.doi.org/10.1371/journal.pone.0034330 Text en Li et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Li, Zhiqing
Cheng, Daojun
Mon, Hiroaki
Tatsuke, Tsuneyuki
Zhu, Li
Xu, Jian
Lee, Jae Man
Xia, Qingyou
Kusakabe, Takahiro
Genome-Wide Identification of Polycomb Target Genes Reveals a Functional Association of Pho with Scm in Bombyx mori
title Genome-Wide Identification of Polycomb Target Genes Reveals a Functional Association of Pho with Scm in Bombyx mori
title_full Genome-Wide Identification of Polycomb Target Genes Reveals a Functional Association of Pho with Scm in Bombyx mori
title_fullStr Genome-Wide Identification of Polycomb Target Genes Reveals a Functional Association of Pho with Scm in Bombyx mori
title_full_unstemmed Genome-Wide Identification of Polycomb Target Genes Reveals a Functional Association of Pho with Scm in Bombyx mori
title_short Genome-Wide Identification of Polycomb Target Genes Reveals a Functional Association of Pho with Scm in Bombyx mori
title_sort genome-wide identification of polycomb target genes reveals a functional association of pho with scm in bombyx mori
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3317521/
https://www.ncbi.nlm.nih.gov/pubmed/22485166
http://dx.doi.org/10.1371/journal.pone.0034330
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