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Flightless-I governs cell fate by recruiting the SUMO isopeptidase SENP3 to distinct HOX genes
被引:14
作者:

Nayak, Arnab
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Goethe Univ Med Sch, Inst Biochem 2, Univ Hosp Bldg 75,Theodor Stern Kai 7, D-60590 Frankfurt, Germany Goethe Univ Med Sch, Inst Biochem 2, Univ Hosp Bldg 75,Theodor Stern Kai 7, D-60590 Frankfurt, Germany

Reck, Anja
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Univ Regensburg, Dept Oral & Maxillofacial Surg, D-93042 Regensburg, Germany Goethe Univ Med Sch, Inst Biochem 2, Univ Hosp Bldg 75,Theodor Stern Kai 7, D-60590 Frankfurt, Germany

Morsczeck, Christian
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Univ Regensburg, Dept Oral & Maxillofacial Surg, D-93042 Regensburg, Germany Goethe Univ Med Sch, Inst Biochem 2, Univ Hosp Bldg 75,Theodor Stern Kai 7, D-60590 Frankfurt, Germany

Mueller, Stefan
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Goethe Univ Med Sch, Inst Biochem 2, Univ Hosp Bldg 75,Theodor Stern Kai 7, D-60590 Frankfurt, Germany Goethe Univ Med Sch, Inst Biochem 2, Univ Hosp Bldg 75,Theodor Stern Kai 7, D-60590 Frankfurt, Germany
机构:
[1] Goethe Univ Med Sch, Inst Biochem 2, Univ Hosp Bldg 75,Theodor Stern Kai 7, D-60590 Frankfurt, Germany
[2] Univ Regensburg, Dept Oral & Maxillofacial Surg, D-93042 Regensburg, Germany
来源:
EPIGENETICS & CHROMATIN
|
2017年
/
10卷
关键词:
Sumoylation;
MLL1/2;
HOX gene;
Mesenchymal stem cells;
Flightless-I;
Chromatin;
SILAC-based proteomics;
HUMAN DENTAL FOLLICLE;
EMBRYONIC STEM-CELLS;
MIXED LINEAGE LEUKEMIA;
OSTEOGENIC DIFFERENTIATION;
CHROMATIN-STRUCTURE;
BIVALENT PROMOTERS;
ESTROGEN-RECEPTOR;
PRECURSOR CELLS;
GROUP PROTEINS;
WOUND REPAIR;
D O I:
10.1186/s13072-017-0122-8
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Background: Despite recent studies on the role of ubiquitin-related SUMO modifier in cell fate decisions, our understanding on precise molecular mechanisms of these processes is limited. Previously, we established that the SUMO isopeptidase SENP3 regulates chromatin assembly of the MLL1/2 histone methyltransferase complex at distinct HOX genes, including the osteogenic master regulator DLX3. A comprehensive mechanism that regulates SENP3 transcriptional function was not understood. Results: Here, we identified flightless-I homolog (FLII), a member of the gelsolin family of actin-remodeling proteins, as a novel regulator of SENP3. We demonstrate that FLII is associated with SENP3 and the MLL1/2 complex. We further show that FLII determines SENP3 recruitment and MLL1/2 complex assembly on the DLX3 gene. Consequently, FLII is indispensible for H3K4 methylation and proper loading of active RNA polymerase II at this gene locus. Most importantly, FLII-mediated SENP3 regulation governs osteogenic differentiation of human mesenchymal stem cells. Conclusion: Altogether, these data reveal a crucial functional interconnection of FLII with the sumoylation machinery that converges on epigenetic regulation and cell fate determination.
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