author_facet Zhang, Zhao
Feng, Jing
Pan, Chenyu
Lv, Xiangdong
Wu, Wenqing
Zhou, Zhaocai
Liu, Feng
Zhang, Lei
Zhao, Yun
Zhang, Zhao
Feng, Jing
Pan, Chenyu
Lv, Xiangdong
Wu, Wenqing
Zhou, Zhaocai
Liu, Feng
Zhang, Lei
Zhao, Yun
author Zhang, Zhao
Feng, Jing
Pan, Chenyu
Lv, Xiangdong
Wu, Wenqing
Zhou, Zhaocai
Liu, Feng
Zhang, Lei
Zhao, Yun
spellingShingle Zhang, Zhao
Feng, Jing
Pan, Chenyu
Lv, Xiangdong
Wu, Wenqing
Zhou, Zhaocai
Liu, Feng
Zhang, Lei
Zhao, Yun
Journal of Cell Biology
Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR
Cell Biology
author_sort zhang, zhao
spelling Zhang, Zhao Feng, Jing Pan, Chenyu Lv, Xiangdong Wu, Wenqing Zhou, Zhaocai Liu, Feng Zhang, Lei Zhao, Yun 1540-8140 0021-9525 Rockefeller University Press Cell Biology http://dx.doi.org/10.1083/jcb.201306012 <jats:p>The evolutionarily conserved Hedgehog (Hh) signaling pathway is transduced by the Cubitus interruptus (Ci)/Gli family of transcription factors that exist in two distinct repressor (CiR/GliR) and activator (CiA/GliA) forms. Aberrant activation of Hh signaling is associated with various human cancers, but the mechanism through which CiR/GliR properly represses target gene expression is poorly understood. Here, we used Drosophila melanogaster and zebrafish models to define a repressor function of Atrophin (Atro) in Hh signaling. Atro directly bound to Ci through its C terminus. The N terminus of Atro interacted with a histone deacetylase, Rpd3, to recruit it to a Ci-binding site at the decapentaplegic (dpp) locus and reduce dpp transcription through histone acetylation regulation. The repressor function of Atro in Hh signaling was dependent on Ci. Furthermore, Rerea, a homologue of Atro in zebrafish, repressed the expression of Hh-responsive genes. We propose that the Atro–Rpd3 complex plays a conserved role to function as a CiR corepressor.</jats:p> Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR Journal of Cell Biology
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series Journal of Cell Biology
source_id 49
title Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR
title_unstemmed Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR
title_full Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR
title_fullStr Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR
title_full_unstemmed Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR
title_short Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR
title_sort atrophin–rpd3 complex represses hedgehog signaling by acting as a corepressor of cir
topic Cell Biology
url http://dx.doi.org/10.1083/jcb.201306012
publishDate 2013
physical 575-583
description <jats:p>The evolutionarily conserved Hedgehog (Hh) signaling pathway is transduced by the Cubitus interruptus (Ci)/Gli family of transcription factors that exist in two distinct repressor (CiR/GliR) and activator (CiA/GliA) forms. Aberrant activation of Hh signaling is associated with various human cancers, but the mechanism through which CiR/GliR properly represses target gene expression is poorly understood. Here, we used Drosophila melanogaster and zebrafish models to define a repressor function of Atrophin (Atro) in Hh signaling. Atro directly bound to Ci through its C terminus. The N terminus of Atro interacted with a histone deacetylase, Rpd3, to recruit it to a Ci-binding site at the decapentaplegic (dpp) locus and reduce dpp transcription through histone acetylation regulation. The repressor function of Atro in Hh signaling was dependent on Ci. Furthermore, Rerea, a homologue of Atro in zebrafish, repressed the expression of Hh-responsive genes. We propose that the Atro–Rpd3 complex plays a conserved role to function as a CiR corepressor.</jats:p>
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author Zhang, Zhao, Feng, Jing, Pan, Chenyu, Lv, Xiangdong, Wu, Wenqing, Zhou, Zhaocai, Liu, Feng, Zhang, Lei, Zhao, Yun
author_facet Zhang, Zhao, Feng, Jing, Pan, Chenyu, Lv, Xiangdong, Wu, Wenqing, Zhou, Zhaocai, Liu, Feng, Zhang, Lei, Zhao, Yun, Zhang, Zhao, Feng, Jing, Pan, Chenyu, Lv, Xiangdong, Wu, Wenqing, Zhou, Zhaocai, Liu, Feng, Zhang, Lei, Zhao, Yun
author_sort zhang, zhao
container_issue 4
container_start_page 575
container_title Journal of Cell Biology
container_volume 203
description <jats:p>The evolutionarily conserved Hedgehog (Hh) signaling pathway is transduced by the Cubitus interruptus (Ci)/Gli family of transcription factors that exist in two distinct repressor (CiR/GliR) and activator (CiA/GliA) forms. Aberrant activation of Hh signaling is associated with various human cancers, but the mechanism through which CiR/GliR properly represses target gene expression is poorly understood. Here, we used Drosophila melanogaster and zebrafish models to define a repressor function of Atrophin (Atro) in Hh signaling. Atro directly bound to Ci through its C terminus. The N terminus of Atro interacted with a histone deacetylase, Rpd3, to recruit it to a Ci-binding site at the decapentaplegic (dpp) locus and reduce dpp transcription through histone acetylation regulation. The repressor function of Atro in Hh signaling was dependent on Ci. Furthermore, Rerea, a homologue of Atro in zebrafish, repressed the expression of Hh-responsive genes. We propose that the Atro–Rpd3 complex plays a conserved role to function as a CiR corepressor.</jats:p>
doi_str_mv 10.1083/jcb.201306012
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institution DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229, DE-D275, DE-Bn3, DE-Brt1, DE-Zwi2, DE-D161
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spelling Zhang, Zhao Feng, Jing Pan, Chenyu Lv, Xiangdong Wu, Wenqing Zhou, Zhaocai Liu, Feng Zhang, Lei Zhao, Yun 1540-8140 0021-9525 Rockefeller University Press Cell Biology http://dx.doi.org/10.1083/jcb.201306012 <jats:p>The evolutionarily conserved Hedgehog (Hh) signaling pathway is transduced by the Cubitus interruptus (Ci)/Gli family of transcription factors that exist in two distinct repressor (CiR/GliR) and activator (CiA/GliA) forms. Aberrant activation of Hh signaling is associated with various human cancers, but the mechanism through which CiR/GliR properly represses target gene expression is poorly understood. Here, we used Drosophila melanogaster and zebrafish models to define a repressor function of Atrophin (Atro) in Hh signaling. Atro directly bound to Ci through its C terminus. The N terminus of Atro interacted with a histone deacetylase, Rpd3, to recruit it to a Ci-binding site at the decapentaplegic (dpp) locus and reduce dpp transcription through histone acetylation regulation. The repressor function of Atro in Hh signaling was dependent on Ci. Furthermore, Rerea, a homologue of Atro in zebrafish, repressed the expression of Hh-responsive genes. We propose that the Atro–Rpd3 complex plays a conserved role to function as a CiR corepressor.</jats:p> Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR Journal of Cell Biology
spellingShingle Zhang, Zhao, Feng, Jing, Pan, Chenyu, Lv, Xiangdong, Wu, Wenqing, Zhou, Zhaocai, Liu, Feng, Zhang, Lei, Zhao, Yun, Journal of Cell Biology, Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR, Cell Biology
title Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR
title_full Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR
title_fullStr Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR
title_full_unstemmed Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR
title_short Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR
title_sort atrophin–rpd3 complex represses hedgehog signaling by acting as a corepressor of cir
title_unstemmed Atrophin–Rpd3 complex represses Hedgehog signaling by acting as a corepressor of CiR
topic Cell Biology
url http://dx.doi.org/10.1083/jcb.201306012