Transcriptome-wide association identifies KLC1 as a regulator of mitophagy in non-syndromic cleft lip with or without palate.

IF 23.7 Q1 MICROBIOLOGY
iMeta Pub Date : 2024-12-20 eCollection Date: 2024-12-01 DOI:10.1002/imt2.262
Shu Lou, Guirong Zhu, Changyue Xing, Shushu Hao, Junyan Lin, Jiayi Xu, Dandan Li, Yifei Du, Congbo Mi, Lian Sun, Lin Wang, Meilin Wang, Mulong Du, Yongchu Pan
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引用次数: 0

Abstract

This study investigated pathogenic genes associated with non-syndromic cleft lip with or without cleft palate (NSCL/P) through transcriptome-wide association studies (TWAS). By integrating expression quantitative trait loci (eQTL) data with genome-wide association study (GWAS) data, we identified key susceptibility genes, including KLC1. Notably, the variant rs12884809 G>A was associated with an increased risk of NSCL/P by enhancing the binding of the transcription factor ELK1 to the KLC1 promoter, thereby activating its expression. This alteration in KLC1 expression subsequently impacted mitophagy, leading to significant changes in cellular behavior and zebrafish morphology. Our findings illuminate the genetic mechanisms underlying NSCL/P and provide valuable insights for future prevention strategies and a deeper understanding of this condition.

全转录组关联确定 KLC1 是非综合征唇裂伴或不伴腭裂患者有丝分裂的调节因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.80
自引率
0.00%
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