Graduate Program in Genetics & Genomics, Baylor College of Medicine, Houston, Texas, United States of America.
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.
PLoS One. 2024 Feb 27;19(2):e0297846. doi: 10.1371/journal.pone.0297846. eCollection 2024.
Johnston's organ, the Drosophila auditory organ, is anatomically very different from the mammalian organ of Corti. However, recent evidence indicates significant cellular and molecular similarities exist between vertebrate and invertebrate hearing, suggesting that Drosophila may be a useful platform to determine the function of the many mammalian deafness genes whose underlying biological mechanisms are poorly characterized. Our goal was a comprehensive screen of all known orthologues of mammalian deafness genes in the fruit fly to better understand conservation of hearing mechanisms between the insect and the fly and ultimately gain insight into human hereditary deafness. We used bioinformatic comparisons to screen previously reported human and mouse deafness genes and found that 156 of them have orthologues in Drosophila melanogaster. We used fluorescent imaging of T2A-GAL4 gene trap and GFP or YFP fluorescent protein trap lines for 54 of the Drosophila genes and found 38 to be expressed in different cell types in Johnston's organ. We phenotypically characterized the function of strong loss-of-function mutants in three genes expressed in Johnston's organ (Cad99C, Msp-300, and Koi) using a courtship assay and electrophysiological recordings of sound-evoked potentials. Cad99C and Koi were found to have significant courtship defects. However, when we tested these genes for electrophysiological defects in hearing response, we did not see a significant difference suggesting the courtship defects were not caused by hearing deficiencies. Furthermore, we used a UAS/RNAi approach to test the function of seven genes and found two additional genes, CG5921 and Myo10a, that gave a statistically significant delay in courtship but not in sound-evoked potentials. Our results suggest that many mammalian deafness genes have Drosophila homologues expressed in the Johnston's organ, but that their requirement for hearing may not necessarily be the same as in mammals.
约翰斯顿器官,果蝇听觉器官,在解剖学上与哺乳动物的科蒂氏器有很大的不同。然而,最近的证据表明,脊椎动物和无脊椎动物的听觉在细胞和分子水平上存在显著的相似性,这表明果蝇可能是一个有用的平台,可以确定许多哺乳动物耳聋基因的功能,这些基因的潜在生物学机制尚未得到很好的描述。我们的目标是对果蝇中所有已知的哺乳动物耳聋基因的直系同源物进行全面筛选,以更好地了解昆虫和果蝇之间听觉机制的保守性,并最终深入了解人类遗传性耳聋。我们使用生物信息学比较筛选了先前报道的人类和小鼠耳聋基因,发现其中 156 个在黑腹果蝇中有直系同源物。我们使用 T2A-GAL4 基因捕获和 GFP 或 YFP 荧光蛋白捕获系的荧光成像对 54 个果蝇基因进行了研究,发现其中 38 个在约翰斯顿器官的不同细胞类型中表达。我们使用交配行为和声音诱发电位的电生理记录,对三个在约翰斯顿器官中表达的强功能缺失突变体(Cad99C、Msp-300 和 Koi)的功能进行了表型特征分析。Cad99C 和 Koi 被发现有明显的交配缺陷。然而,当我们测试这些基因在听觉反应中的电生理缺陷时,我们没有发现显著的差异,这表明交配缺陷不是由听力缺陷引起的。此外,我们使用 UAS/RNAi 方法测试了七个基因的功能,发现另外两个基因,CG5921 和 Myo10a,在交配行为上有明显的延迟,但在声音诱发电位上没有明显的差异。我们的结果表明,许多哺乳动物耳聋基因在果蝇的约翰斯顿器官中有同源物表达,但它们对听觉的需求不一定与哺乳动物相同。