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小鼠同源盒基因Cdx1的破坏通过改变Hox基因的中胚层表达域来影响中轴骨骼特征。

Disruption of the murine homeobox gene Cdx1 affects axial skeletal identities by altering the mesodermal expression domains of Hox genes.

作者信息

Subramanian V, Meyer B I, Gruss P

机构信息

Department of Molecular Cell Biology, Max Planck Institute for Biophysical Chemistry, Göttingen, Federal Republic of Germany.

出版信息

Cell. 1995 Nov 17;83(4):641-53. doi: 10.1016/0092-8674(95)90104-3.

Abstract

Cdx1 is expressed along the embryonic axis from day 7.5 postcoitum until day 12, by which time the anterior limit of expression has regressed from the hindbrain level to the forelimb bud region. To assign a functional role for Cdx1 in murine embryonic development, we have inactivated the gene via homologous recombination. Viable fertile homozygous mutant mice were obtained that show anterior homeotic transformations of vertebrae. These abnormalities were concomitant with posterior shifts of Hox gene expression domains in the somitic mesoderm. The presence of putative Cdx1-binding sites in Hox gene control regions as well as in vitro transactivation of Hoxa-7 indicates a direct regulation.

摘要

Cdx1在胚胎期从妊娠后7.5天到12天沿胚胎轴表达,到此时其表达的前界已从后脑水平退缩到前肢芽区域。为了确定Cdx1在小鼠胚胎发育中的功能作用,我们通过同源重组使该基因失活。获得了有活力且可育的纯合突变小鼠,这些小鼠表现出椎骨的前部同源异型转化。这些异常与体节中胚层中Hox基因表达域的后移同时出现。Hox基因控制区域中存在假定的Cdx1结合位点以及Hoxa - 7的体外反式激活表明存在直接调控。

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