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在缺乏Sp6的小鼠中,多个器官和附属器的发育受到损害。

The development of several organs and appendages is impaired in mice lacking Sp6.

作者信息

Hertveldt Valérie, Louryan Stéphane, van Reeth Thierry, Drèze Pierre, van Vooren Pascale, Szpirer Josiane, Szpirer Claude

机构信息

Université libre de Bruxelles, Institut de Biologie et de Médecine Moléculaires, Rue Profs Jeener & Brachet, 12, B-6041 Gosselies (Charleroi), Belgium.

出版信息

Dev Dyn. 2008 Apr;237(4):883-92. doi: 10.1002/dvdy.21355.

Abstract

SP6 belongs to the SP/KLF family of transcription factors, characterized by a DNA-binding domain composed of three zinc fingers of the C(2)H(2) type. The Sp6 gene generates two different transcripts, termed Sp6 and epiprofin, which differ in the first exon and encode the same SP6 protein. These transcripts are mainly expressed in the skin, the teeth, and the limb buds of embryos and also in the adult lungs. To gain insight into the biological function of the SP6 protein, we knocked out the gene by eliminating the full coding region. The resulting Sp6 null mice are nude, lack functional teeth, and present limb and lung malformations. We also showed that the identified abnormalities are associated with apoptotic misregulations. In conclusion, this work indicates that Sp6 plays a critical role in the development of several epithelium-containing organs or appendages, possibly by regulating apoptosis.

摘要

SP6属于转录因子的SP/KLF家族,其特征是具有一个由三个C(2)H(2)型锌指组成的DNA结合结构域。Sp6基因产生两种不同的转录本,分别称为Sp6和表皮素,它们在第一个外显子上有所不同,但编码相同的SP6蛋白。这些转录本主要在胚胎的皮肤、牙齿和肢芽中表达,在成年肺中也有表达。为了深入了解SP6蛋白的生物学功能,我们通过消除完整的编码区域敲除了该基因。产生的Sp6基因敲除小鼠是裸鼠,没有功能性牙齿,并且存在肢体和肺部畸形。我们还表明,所发现的异常与凋亡调控异常有关。总之,这项工作表明Sp6可能通过调节凋亡在几个含上皮器官或附属器的发育中起关键作用。

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