一种新的小鼠耳聋基因Pejvakin突变分析。

IF 2.8 4区 生物学 Q2 DEVELOPMENTAL BIOLOGY
genesis Pub Date : 2026-01-20 DOI:10.1002/dvg.70041
Maria Teresa Marcos-Almaraz, Rebeca Llorente Aparicio, Iris López-Hernández, Csaba Harasztosi, Marlies Knipper, Lukas Rüttiger, Wibke Singer, Miguel Angel de la Fuente, Thomas Schimmang
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引用次数: 0

摘要

Pejvakin (Pjvk)基因的功能丧失与细胞应激引起的耳聋有关。这被认为是由于过氧化物酶体生物发生缺陷造成的。在这里,我们描述了一种缺乏Pjvk编码区外显子3的新型小鼠突变。携带这种突变的小鼠突变体显示出与深度耳聋和外毛细胞功能降低相关的毛细胞损失。携带Pjvk外显子3缺失的细胞系显示氧化应激时过氧化物酶过氧化氢酶上调。为了进一步明确Pjvk的定位,我们在其cDNA中引入了氨基和羧基末端标签,这些标签未能确认其存在于过氧化物酶体中,但可能是由于蛋白质的错误靶向。因此,我们的研究证实了Pjvk对维持毛细胞和完整听力的需求,以及在细胞应激时过氧化物酶体的特定作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of a Novel Mouse Mutation of the Deafness Gene Pejvakin

Loss of function of the Pejvakin (Pjvk) gene has been associated with deafness induced by cellular stress. This has been postulated to occur due to defective peroxisome biogenesis. Here, we have characterized a novel mouse mutation lacking exon 3 of the Pjvk coding region. A mouse mutant carrying this mutation showed loss of hair cells associated with profound deafness and reduced outer hair cell function. A cell line carrying a deletion of Pjvk exon 3 revealed upregulation of the peroxisomal enzyme catalase upon oxidative stress. In order to further clarify the localization of Pjvk, we introduced amino- and carboxy-terminal tags in its cDNA which failed to confirm its presence in peroxisomes but is likely to be due to mis-targeting of the protein. Our study thus confirms the requirement of Pjvk for maintenance of hair cells and intact hearing and a specific role in peroxisomes upon exposure to cellular stress.

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来源期刊
genesis
genesis 生物-发育生物学
CiteScore
3.60
自引率
0.00%
发文量
40
审稿时长
6-12 weeks
期刊介绍: As of January 2000, Developmental Genetics was renamed and relaunched as genesis: The Journal of Genetics and Development, with a new scope and Editorial Board. The journal focuses on work that addresses the genetics of development and the fundamental mechanisms of embryological processes in animals and plants. With increased awareness of the interplay between genetics and evolutionary change, particularly during developmental processes, we encourage submission of manuscripts from all ecological niches. The expanded numbers of genomes for which sequencing is being completed will facilitate genetic and genomic examination of developmental issues, even if the model system does not fit the “classical genetic” mold. Therefore, we encourage submission of manuscripts from all species. Other areas of particular interest include: 1) the roles of epigenetics, microRNAs and environment on developmental processes; 2) genome-wide studies; 3) novel imaging techniques for the study of gene expression and cellular function; 4) comparative genetics and genomics and 5) animal models of human genetic and developmental disorders. genesis presents reviews, full research articles, short research letters, and state-of-the-art technology reports that promote an understanding of the function of genes and the roles they play in complex developmental processes.
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