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首页> 外文期刊>The Journal of biological chemistry >High Temperature Requirement Factor A1 (HTRA1) Gene Regulates Angiogenesis through Transforming Growth Factor-β Family Member Growth Differentiation Factor 6
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High Temperature Requirement Factor A1 (HTRA1) Gene Regulates Angiogenesis through Transforming Growth Factor-β Family Member Growth Differentiation Factor 6

机译:高温需求因子A1(HTRA1)基因通过转化生长因子-β家族成员生长分化因子6来调节血管生成

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Genome-wide association study (GWAS) has identified genetic variants in the promoter region of the high temperature requirement factor A1 (HTRA1) gene associated with age-related macular degeneration (AMD). As a secreted serine protease, HTRA1 has been reported to interact with members of the transforming growth factor-β (TGF-β) family and regulate their signaling pathways. Growth differentiation factor 6 (GDF6), a member of the TGF-β family, is involved in ectoderm patterning and eye development. Mutations in GDF6 have been associated with abnormal eye development that may result in microphthalmia and anophthalmia. In this report, we identified a single nucleotide polymorphism (SNP) rs6982567 A/G near the GDF6 gene that is significantly associated with AMD (p value = 3.54 × 10?8). We demonstrated that the GDF6 AMD risk allele (rs6982567 A) is associated with decreased expression of the GDF6 and increased expression of HTRA1. Similarly, the HTRA1 AMD risk allele (rs10490924 T) is associated with decreased GDF6 and increased HTRA1 expression. We observed decreased vascular development in the retina and significant up-regulation of GDF6 gene in the RPE layer, retinal and brain tissues in HTRA1 knock-out (htra1?/?) mice as compared with the wild-type counterparts. Furthermore, we showed enhanced SMAD signaling in htra1?/? mice. Our data suggests a critical role of HTRA1 in the regulation of angiogenesis via TGF-β signaling and identified GDF6 as a novel disease gene for AMD.
机译:基因组 - 宽协会研究(GWAS)已经确定了与年龄相关性黄斑变性(AMD)相关的高温要求因子A1(HTRA1)基因的启动子区的遗传变体。作为分泌的丝氨酸蛋白酶,已经报道了HTRA1与转化生长因子-β(TGF-β)家族的成员相互作用并调节其信号通路。生长分化因子6(GDF6)是TGF-β家族的成员,涉及Ectoderm图案化和眼睛发育。 GDF6中的突变与可能导致微蛋白和咽喉的异常眼发育有关。在本报告中,我们鉴定了与AMD显着相关的GDF6基因附近的单个核苷酸多态性(SNP)RS6982567A / g(P值= 3.54×10?8)。我们证明GDF6 AMD风险等位基因(RS6982567A)与GDF6的表达降低以及HTRA1的表达增加有关。类似地,HTRA1 AMD风险等位基因(RS10490924 T)与GDF6降低和HTRA1表达增加有关。在与野生型对应物相比,我们观察到视网膜,视网膜层,视网膜和脑组织中的GDF6基因的显着上调。与野生型对应相比,在RPE层,视网膜和脑组织中的显着上调。此外,我们在HTRA1中显示了增强的SMAD信号传导?/?老鼠。我们的数据表明HTRA1在通过TGF-β信号传导调节血管生成调节的关键作用,并将GDF6鉴定为AMD的新型疾病基因。

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