Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis, CA 95616.
Department of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California, Davis, CA 95616.
Proc Natl Acad Sci U S A. 2017 Oct 24;114(43):11476-11481. doi: 10.1073/pnas.1709082114. Epub 2017 Oct 11.
Chondrodystrophy in dogs is defined by dysplastic, shortened long bones and premature degeneration and calcification of intervertebral discs. Independent genome-wide association analyses for skeletal dysplasia (short limbs) within a single breed ( = 0.01) and intervertebral disc disease (IVDD) across breeds ( = 4.0 × 10) both identified a significant association to the same region on CFA12. Whole genome sequencing identified a highly expressed retrogene within this shared region. The retrogene segregated with limb length and had an odds ratio of 51.23 (95% CI = 46.69, 56.20) for IVDD. Long bone length in dogs is a unique example of multiple disease-causing retrocopies of the same parental gene in a mammalian species. FGF signaling abnormalities have been associated with skeletal dysplasia in humans, and our findings present opportunities for both selective elimination of a medically and financially devastating disease in dogs and further understanding of the ever-growing complexity of retrogene biology.
犬的软骨发育不良症表现为长骨畸形、缩短,以及椎间盘的过早退变和钙化。在单一品种中对骨骼发育不良(短肢)进行独立的全基因组关联分析( = 0.01),以及对跨品种的椎间盘疾病(IVDD)进行分析( = 4.0×10),都在 CFA12 上发现了与同一区域的显著关联。全基因组测序在这个共享区域内鉴定出一个高度表达的反转录基因。该反转录基因与肢体长度相关,IVDD 的优势比为 51.23(95%CI = 46.69,56.20)。在哺乳动物中,犬的长骨长度是同一亲本基因的多个致病反转录基因的一个独特例子。FGF 信号异常与人类的骨骼发育不良有关,我们的发现为选择性消除犬类中具有医疗和经济破坏性的疾病提供了机会,并进一步了解不断增长的反转录基因生物学的复杂性。