4.6 Article

Zinc finger transcription factor Sp7/Osterix acts on bone formation and regulates col10a1a expression in zebrafish

期刊

SCIENCE BULLETIN
卷 62, 期 3, 页码 174-184

出版社

ELSEVIER
DOI: 10.1016/j.scib.2017.01.009

关键词

Sp7/Osterix; col10a1a; Osteoblast; Opercula; TALEN; Zebrafish

资金

  1. National High Technology Research and Development Program of China [2011AA100402-2]
  2. National Natural Science Foundation of China (NSFC) [31271356, 31030062, 81070455]
  3. National Basic Research Program of China [2012CB947600]
  4. Jiangsu Distinguished Professorship Program [SR13400111]
  5. Natural Science Foundation of Jiangsu Province [BK2012052]
  6. Priority Academic Program Development (PAPD) of Jiangsu Higher Education Institutions [YX13400214]
  7. High-Level Innovative Team of Jiangsu Province
  8. 333 project of Jiangsu Province [BRA2015328]

向作者/读者索取更多资源

Sp7/Osterix as a zinc finger transcription factor is expressed specifically in osteoblasts. Embryonic lethality of Sp7 knockout mice, however, has prevented from examining the functions of Sp7 in osteoblast and bone formation in live animals. Here we used TALEN, a versatile genome-editing tool, to generate one zebrafish sp7 mutant line. Homozygous sp7-/- mutant zebrafish are able to survive to adulthood. Alizarin Red staining and Micro-CT analysis showed that sp7-/- larvae and adult fish fail to develop normal opercula, and display curved tail fins and severe craniofacial malformation, while Alcian Blue staining showed no obvious cartilage defects in sp7-/- fish. Quantitative RT-PCR showed that a number of osteoblast markers including spp1, phex, col1ala, and col1a1b are significantly down-regulated in sp7-/- fish. Furthermore, col10a1a, whose ortholog is the cartilage marker in mice, was shown to be a novel downstream gene of Sp7 as an osteoblast marker in zebrafish. Together, these results suggest that Sp7 is required for zebrafish bone development and zebrafish sp7 mutants provide animal models for investigating novel aspects of bone development. (C) 2017 Science China Press. Published by Elsevier B.V. and Science China Press. All rights reserved.

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