Yamada M, Revelli J P, Eichele G, Barron M, Schwartz R J
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas, 77030, USA.
Dev Biol. 2000 Dec 1;228(1):95-105. doi: 10.1006/dbio.2000.9927.
Expression patterns of Tbx2, -3, and -5 genes were analyzed during chick embryonic heart development. Transcripts of these three cTbx genes were detected in overlapping patterns in the early cardiac crescent. cTbx2 and cTbx3 expression patterns closely overlapped with that of bmp2. cTbx5 expression diverged from cTbx2 and bmp2 during the elaboration and folding of the heart tube. In comparison, cTbx2 expression overlapped significantly with that of bmp2 and bmp4 during all stages of heart development and during later embryonic stages, suggestive of a specialized role for Tbx2 in septation. Coexpression of cTbx 2 and cTbx3 genes with bmp2 transcripts raised the possibility that these cTbx genes might be downstream bmp2 targets. Application of bmp2 selectively induced cTbx2 and cTbx3 expression in noncardiogenic embryonic tissue, and the bmp antagonist Noggin down-regulated cTbx2 gene activity. Moreover, the appearance of murine mTbx2 was blocked in bmp2 null mouse embryos. cTbx2 and to a lesser extent cTbx3 gene activity appears to be directed by BMPs during early cardiogenesis.
在鸡胚心脏发育过程中分析了Tbx2、-3和-5基因的表达模式。这三个鸡Tbx基因的转录本在早期心脏新月区以重叠模式被检测到。cTbx2和cTbx3的表达模式与bmp2的表达模式紧密重叠。在心脏管的形成和折叠过程中,cTbx5的表达与cTbx2和bmp2的表达有所不同。相比之下,在心脏发育的所有阶段以及胚胎后期,cTbx2的表达与bmp2和bmp4的表达显著重叠,提示Tbx2在分隔中具有特殊作用。cTbx 2和cTbx3基因与bmp2转录本的共表达增加了这些cTbx基因可能是bmp2下游靶点的可能性。在非心脏源性胚胎组织中,bmp2的应用选择性地诱导了cTbx2和cTbx3的表达,而bmp拮抗剂Noggin下调了cTbx2基因的活性。此外,在bmp2基因敲除的小鼠胚胎中,小鼠mTbx2的出现受到了阻碍。在早期心脏发生过程中,cTbx2以及程度较轻的cTbx3基因活性似乎受骨形态发生蛋白(BMPs)的调控。