Prdm5 Regulates Collagen Gene Transcription by Association with RNA Polymerase II in Developing Bone

被引:46
作者
Galli, Giorgio Giacomo [1 ,2 ]
de Lichtenberg, Kristian Honnens [1 ,2 ]
Carrara, Matteo [3 ]
Hans, Wolfgang [4 ]
Wuelling, Manuela [5 ]
Mentz, Bettina [1 ,2 ]
Multhaupt, Hinke Arnolda [6 ,7 ]
Fog, Cathrine Kolster [1 ,2 ]
Jensen, Klaus Thorleif [1 ,2 ]
Rappsilber, Juri [8 ]
Vortkamp, Andrea [5 ]
Coulton, Les [9 ]
Fuchs, Helmut [5 ]
Gailus-Durner, Valerie [4 ]
de Angelis, Martin Hrabe [4 ,10 ]
Calogero, Raffaele Adolfo [3 ]
Couchman, John Robert [6 ,7 ]
Lund, Anders Henrik [1 ,2 ]
机构
[1] Univ Copenhagen, Biotech Res & Innovat Ctr, Copenhagen, Denmark
[2] Univ Copenhagen, Ctr Epigenet, Copenhagen, Denmark
[3] Univ Turin, Dept Clin & Biol Sci, Ctr Mol Biotechnol, Turin, Italy
[4] German Res Ctr Environm Hlth GmbH, Helmholtz Zentrum Munchen, Inst Expt Genet, German Mouse Clin, Neuherberg, Germany
[5] Univ Duisburg Essen, Ctr Med Biotechnol, Dept Dev Biol, Essen, Germany
[6] Univ Copenhagen, Dept Biomed Sci, Copenhagen, Denmark
[7] Univ Copenhagen, BRIC, Copenhagen, Denmark
[8] Univ Edinburgh, Wellcome Trust Ctr Cell Biol, Edinburgh, Midlothian, Scotland
[9] Univ Sheffield, Sch Med, Acad Unit Bone Biol, Sheffield, S Yorkshire, England
[10] Chair Expt Genet TUM, Freising Weihenstephan, Germany
基金
新加坡国家研究基金会; 英国惠康基金;
关键词
BRITTLE CORNEA SYNDROME; TARGETED DISRUPTION; 1ST INTRON; EXPRESSION; FAMILY; CONTAINS; PATHWAY; PROTEIN;
D O I
10.1371/journal.pgen.1002711
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
PRDM family members are transcriptional regulators involved in tissue specific differentiation. PRDM5 has been reported to predominantly repress transcription, but a characterization of its molecular functions in a relevant biological context is lacking. We demonstrate here that Prdm5 is highly expressed in developing bones; and, by genome-wide mapping of Prdm5 occupancy in pre-osteoblastic cells, we uncover a novel and unique role for Prdm5 in targeting all mouse collagen genes as well as several SLRP proteoglycan genes. In particular, we show that Prdm5 controls both Collagen I transcription and fibrillogenesis by binding inside the Col1a1 gene body and maintaining RNA polymerase II occupancy. In vivo, Prdm5 loss results in delayed ossification involving a pronounced impairment in the assembly of fibrillar collagens. Collectively, our results define a novel role for Prdm5 in sustaining the transcriptional program necessary to the proper assembly of osteoblastic extracellular matrix.
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页数:13
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