COX4-like, a Nuclear-Encoded Mitochondrial Gene Duplicate, Is Essential for Male Fertility in Drosophila melanogaster

被引:7
|
作者
Eslamieh, Mohammadmehdi [1 ]
Mirsalehi, Ayda [1 ]
Markova, Dragomira N. [1 ]
Betran, Esther [1 ]
机构
[1] Univ Texas Arlington, Dept Biol, Arlington, TX 76019 USA
基金
美国国家卫生研究院;
关键词
nuclear-encoded mitochondrial gene; gene duplication; CRISPR knockout; COX4L; spermatogenesis; Drosophila melanogaster; CYTOCHROME-C-OXIDASE; EVOLUTIONARY RATE COVARIATION; PROCESSING PEPTIDASE; MAXIMUM-LIKELIHOOD; PROTEIN IMPORT; SELECTION; CONFLICT; ACCURACY; SUBUNITS; PLATFORM;
D O I
10.3390/genes13030424
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Recent studies on nuclear-encoded mitochondrial genes (N-mt genes) in Drosophila melanogaster have shown a unique pattern of expression for newly duplicated N-mt genes, with many duplicates having a testis-biased expression and playing an essential role in spermatogenesis. In this study, we investigated a newly duplicated N-mt gene-i.e., Cytochrome c oxidase 4-like (COX4L)-in order to understand its function and, consequently, the reason behind its retention in the D. melanogaster genome. The COX4L gene is a duplicate of the Cytochrome c oxidase 4 (COX4) gene of OXPHOS complex IV. While the parental COX4 gene has been found in all eukaryotes, including single-cell eukaryotes such as yeast, we show that COX4L is only present in the Brachycera suborder of Diptera; thus, both genes are present in all Drosophila species, but have significantly different patterns of expression: COX4 is highly expressed in all tissues, while COX4L has a testis-specific expression. To understand the function of this new gene, we first knocked down its expression in the D. melanogaster germline using two different RNAi lines driven by the bam-Gal4 driver; second, we created a knockout strain for this gene using CRISPR-Cas9 technology. Our results showed that knockdown and knockout lines of COX4L produce partial sterility and complete sterility in males, respectively, where a lack of sperm individualization was observed in both cases. Male infertility was prevented by driving COX4L-HA in the germline, but not when driving COX4-HA. In addition, ectopic expression of COX4L in the soma caused embryonic lethality, while overexpression in the germline led to a reduction in male fertility. COX4L-KO mitochondria show reduced membrane potential, providing a plausible explanation for the male sterility observed in these flies. This prominent loss-of-function phenotype, along with its testis-biased expression and its presence in the Drosophila sperm proteome, suggests that COX4L is a paralogous, specialized gene that is assembled in OXPHOS complex IV of male germline cells and/or sperm mitochondria.
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页数:16
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