A muscle-specific promoter directs Pitx3 gene expression in skeletal muscle cells

被引:25
作者
Coulon, Vincent
L'Honore, Aurore
Ouimette, Jean-Francois
Dumontier, Emilie
van den Munckhof, Pepijn
Drouin, Jacques
机构
[1] Inst Rech Clin Montreal, Lab Genet Mol, Montreal, PQ H2W 1R7, Canada
[2] Inst Mol Genet, CNRS, UMR 5535, F-34293 Montpellier 05, France
[3] Univ Amsterdam, Acad Med Centrum, NL-1100 DD Amsterdam, Netherlands
关键词
D O I
10.1074/jbc.M706119200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The Pitx homeobox transcription factor genes have been implicated in different developmental processes, including determination of hind limb identity for Pitx1, left-right asymmetry for Pitx2, and eye development and survival of midbrain dopaminergic neurons for Pitx3. Pitx1 and Pitx2 have partly redundant activities in craniofacial development, including in pituitary organogenesis, as indicated by their names. These genes also exhibit redundant activities in the control of hind limb bud growth. Recent studies have shown expression of the three Pitx genes in muscle, with Pitx3 being the most widely expressed in all skeletal muscles. We now report the identification of a muscle-specific promoter within the Pitx3 gene that is situated between the first exon for eye and brain expression and exon 2 that contains the initiator ATG codon. Sequences proximal to this muscle-specific exon 1 are essential and sufficient to confer muscle-specific expression in transgenic mice, they are responsive to myogenic basic helix-loop-helix regulatory factors, and they recruit these factors in vivo. In agreement with exclusive use of the muscle-specific promoter in aphakia mice that are deleted of the brain promoter, the trimethyl-lysine 4 histone H3 promoter signature shifts to this promoter in embryonic day 13 ak limb bud muscle cells. Myogenic basic helix-loop-helix regulatory factor activation of Pitx3 transcription may be part of a positive feedback loop contributing to establishment of the myogenic program.
引用
收藏
页码:33192 / 33200
页数:9
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