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一种系统遗传学方法确定了蛋白酶体因子在心脏发育和先天性心脏病中的作用。

A systems genetics approach identifies roles for proteasome factors in heart development and congenital heart defects.

作者信息

Farr Gist H, Reid Whitaker, Hasegawa Eva H, Azzam Azzam, Young Isabelle, Li Mona L, Olson Aaron K, Beier David R, Maves Lisa

机构信息

Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, United States of America.

University of Washington, Seattle, Washington, United States of America.

出版信息

PLoS Genet. 2025 Aug 26;21(8):e1011579. doi: 10.1371/journal.pgen.1011579. eCollection 2025 Aug.

Abstract

Congenital heart defects (CHDs) occur in about 1% of live births and are the leading cause of infant death due to birth defects. While there have been remarkable efforts to pursue large-scale whole-exome and genome sequencing studies on CHD patient cohorts, it is estimated that these approaches have thus far accounted for only about 50% of the genetic contribution to CHDs. We sought to take a new approach to identify genetic causes of CHDs. By combining analyses of genes that are under strong selective constraint along with published embryonic heart transcriptomes, we identified over 200 new candidate genes for CHDs. We utilized protein-protein interaction (PPI) network analysis to identify a functionally-related subnetwork consisting of known CHD genes as well as genes encoding proteasome factors, in particular POMP, PSMA6, PSMA7, PSMD3, and PSMD6. We used CRISPR targeting in zebrafish embryos to preliminarily identify roles for the PPI subnetwork genes in heart development. We then used CRISPR to create new mutant zebrafish strains for two of the proteasome genes in the subnetwork: pomp and psmd6. We show that loss of proteasome gene functions leads to defects in zebrafish heart development, including dysmorphic hearts, myocardial cell blebbing, and reduced outflow tracts. We also identified deficits in cardiac function in pomp and psmd6 mutants. These heart defects resemble those seen in zebrafish mutants for known CHD genes and other critical heart development genes. Our study provides a novel systems genetics approach to further our understanding of the genetic causes of human CHDs.

摘要

先天性心脏病(CHD)在活产婴儿中的发生率约为1%,是出生缺陷导致婴儿死亡的主要原因。尽管已经付出了巨大努力对先天性心脏病患者队列进行大规模全外显子组和基因组测序研究,但据估计,到目前为止,这些方法仅解释了约50%的先天性心脏病遗传因素。我们试图采用一种新方法来确定先天性心脏病的遗传原因。通过结合对处于强选择约束下的基因分析以及已发表的胚胎心脏转录组,我们确定了200多个新的先天性心脏病候选基因。我们利用蛋白质-蛋白质相互作用(PPI)网络分析,确定了一个功能相关的子网,该子网由已知的先天性心脏病基因以及编码蛋白酶体因子的基因组成,特别是POMP、PSMA6、PSMA7、PSMD3和PSMD6。我们在斑马鱼胚胎中使用CRISPR靶向技术,初步确定PPI子网基因在心脏发育中的作用。然后,我们使用CRISPR为子网中的两个蛋白酶体基因创建新的斑马鱼突变品系:pomp和psmd6。我们发现蛋白酶体基因功能丧失会导致斑马鱼心脏发育缺陷,包括心脏畸形、心肌细胞起泡和流出道减少。我们还确定了pomp和psmd6突变体的心脏功能缺陷。这些心脏缺陷类似于已知先天性心脏病基因和其他关键心脏发育基因的斑马鱼突变体中出现的缺陷。我们的研究提供了一种新的系统遗传学方法,以加深我们对人类先天性心脏病遗传原因的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a15/12404643/de3f51df7f25/pgen.1011579.g001.jpg

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