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牛身上的无毛条纹表明TSR2与早期毛囊形成有关。

Hairless Streaks in Cattle Implicate TSR2 in Early Hair Follicle Formation.

作者信息

Murgiano Leonardo, Shirokova Vera, Welle Monika Maria, Jagannathan Vidhya, Plattet Philippe, Oevermann Anna, Pienkowska-Schelling Aldona, Gallo Daniele, Gentile Arcangelo, Mikkola Marja, Drögemüller Cord

机构信息

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bern, Switzerland; DermFocus, University of Bern, Bern, Switzerland.

Developmental Biology Program, Institute of Biotechnology, University of Helsinki, Helsinki, Finland.

出版信息

PLoS Genet. 2015 Jul 23;11(7):e1005427. doi: 10.1371/journal.pgen.1005427. eCollection 2015 Jul.

Abstract

Four related cows showed hairless streaks on various parts of the body with no correlation to the pigmentation pattern. The stripes occurred in a consistent pattern resembling the lines of Blaschko. The non-syndromic hairlessness phenotype observed occurred across three generations of a single family and was compatible with an X-linked mode of inheritance. Linkage analysis and subsequent whole genome sequencing of one affected female identified two perfectly associated non-synonymous sequence variants in the critical interval on bovine chromosome X. Both variants occurred in complete linkage disequilibrium and were absent in more than 3900 controls. An ERCC6L missense mutation was predicted to cause an amino acid substitution of a non-conserved residue. Analysis in mice showed no specific Ercc6l expression pattern related to hair follicle development and therefore ERCC6L was not considered as causative gene. A point mutation at the 5'-splice junction of exon 5 of the TSR2, 20S rRNA accumulation, homolog (S. cerevisiae), gene led to the production of two mutant transcripts, both of which contain a frameshift and generate a premature stop codon predicted to truncate approximately 25% of the protein. Interestingly, in addition to the presence of both physiological TSR2 transcripts, the two mutant transcripts were predominantly detected in the hairless skin of the affected cows. Immunohistochemistry, using an antibody against the N-terminal part of the bovine protein demonstrated the specific expression of the TSR2 protein in the skin and the hair of the affected and the control cows as well as in bovine fetal skin and hair. The RNA hybridization in situ showed that Tsr2 was expressed in pre- and post-natal phases of hair follicle development in mice. Mammalian TSR2 proteins are highly conserved and are known to be broadly expressed, but their precise in vivo functions are poorly understood. Thus, by dissecting a naturally occurring mutation in a domestic animal species, we identified TSR2 as a regulator of hair follicle development.

摘要

四头相关的奶牛在身体的不同部位出现无毛条纹,与色素沉着模式无关。这些条纹以一种与布拉斯科线相似的一致模式出现。在一个单一家庭的三代中观察到的非综合征性无毛表型与X连锁遗传模式相符。对一头受影响的雌性奶牛进行连锁分析和随后的全基因组测序,在牛X染色体的关键区间鉴定出两个完全相关的非同义序列变异。这两个变异处于完全连锁不平衡状态,在超过3900个对照中均未出现。预测一个ERCC6L错义突变会导致一个非保守残基的氨基酸替换。在小鼠中的分析表明,没有与毛囊发育相关的特定Ercc6l表达模式,因此ERCC6L不被认为是致病基因。TSR2,20S核糖体RNA积累,同源物(酿酒酵母)基因外显子5的5'-剪接连接处的一个点突变导致产生两种突变转录本,这两种转录本都包含移码并产生一个预测会截断约25%蛋白质的过早终止密码子。有趣的是,除了存在两种生理性TSR2转录本外,这两种突变转录本在受影响奶牛的无毛皮肤中大量检测到。使用针对牛蛋白N端部分抗体的免疫组织化学显示,TSR2蛋白在受影响奶牛和对照奶牛的皮肤和毛发以及牛胎儿皮肤和毛发中特异性表达。原位RNA杂交表明,Tsr2在小鼠毛囊发育的产前和产后阶段均有表达。哺乳动物TSR2蛋白高度保守,已知广泛表达,但其确切的体内功能尚不清楚。因此,通过剖析家畜物种中自然发生的突变,我们确定TSR2是毛囊发育的调节因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a7b/4512707/5fe74a0791b3/pgen.1005427.g001.jpg

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