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一种新的 MYH7 种系突变导致猪进行性显性肌病。

A de novo germline mutation in MYH7 causes a progressive dominant myopathy in pigs.

机构信息

Institute of Genetics, Vetsuisse Faculty, University of Bern, Bremgartenstrasse 109a, Bern, 3001, Switzerland.

出版信息

BMC Genet. 2012 Nov 15;13:99. doi: 10.1186/1471-2156-13-99.

Abstract

BACKGROUND

About 9% of the offspring of a clinically healthy Piétrain boar named 'Campus' showed a progressive postural tremor called Campus syndrome (CPS). Extensive backcross experiments suggested a dominant mode of inheritance, and the founder boar was believed to be a gonadal mosaic. A genome-scan mapped the disease-causing mutation to an 8 cM region of porcine chromosome 7 containing the MHY7 gene. Human distal myopathy type 1 (MPD1), a disease partially resembling CPS in pigs, has been associated with mutations in the MYH7 gene.

RESULTS

The porcine MYH7 gene structure was predicted based on porcine reference genome sequence, porcine mRNA, and in comparison to the human ortholog. The gene structure was highly conserved with the exception of the first exon. Mutation analysis of a contiguous genomic interval of more than 22 kb spanning the complete MYH7 gene revealed an in-frame insertion within exon 30 of MYH7 (c.4320_4321insCCCGCC) which was perfectly associated with the disease phenotype and confirmed the dominant inheritance. The mutation is predicted to insert two amino acids (p.Ala1440_Ala1441insProAla) in a very highly conserved region of the myosin tail. The boar 'Campus' was shown to be a germline and somatic mosaic as assessed by the presence of the mutant allele in seven different organs.

CONCLUSION

This study illustrates the usefulness of recently established genomic resources in pigs. We have identified a spontaneous mutation in MYH7 as the causative mutation for CPS. This paper describes the first case of a disorder caused by a naturally occurring mutation in the MYH7 gene of a non-human mammalian species. Our study confirms the previous classification as a primary myopathy and provides a defined large animal model for human MPD1. We provide evidence that the CPS mutation occurred during the early development of the boar 'Campus'. Therefore, this study provides an example of germline mosaicism with an asymptomatic founder.

摘要

背景

大约 9%的一只有名的皮特兰公猪“校园”的后代表现出一种进行性姿势震颤,称为校园综合征(CPS)。广泛的回交实验表明,该疾病以显性模式遗传,并且该创始公猪被认为是生殖腺嵌合体。全基因组扫描将致病突变定位到包含 MHY7 基因的猪 7 号染色体的 8cM 区域。人类远端肌病 1 型(MPD1),一种在猪中部分类似于 CPS 的疾病,与 MYH7 基因的突变有关。

结果

根据猪参考基因组序列、猪 mRNA 并与人类同源物进行比较,预测了猪 MYH7 基因结构。基因结构高度保守,除了第一个外显子。对跨越完整 MYH7 基因的超过 22kb 的连续基因组间隔进行突变分析,发现 MYH7 外显子 30 内的框内插入(c.4320_4321insCCCGCC),该突变与疾病表型完全相关,并证实了显性遗传。该突变预计会在肌球蛋白尾部的一个高度保守区域插入两个氨基酸(p.Ala1440_Ala1441insProAla)。通过在七个不同器官中存在突变等位基因,证明了公猪“校园”是生殖系和体细突变的嵌合体。

结论

本研究说明了最近在猪中建立的基因组资源的有用性。我们已经确定了 MYH7 中的自发突变是 CPS 的致病突变。本文描述了首例由非人类哺乳动物的 MYH7 基因中自然发生的突变引起的疾病。我们的研究证实了之前作为原发性肌病的分类,并为人类 MPD1 提供了明确的大型动物模型。我们提供的证据表明 CPS 突变发生在公猪“校园”的早期发育过程中。因此,本研究提供了一个生殖系嵌合体的无症状创始者的例子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d755/3542579/87da439dfeab/1471-2156-13-99-1.jpg

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