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Different expression patterns of sperm motility-related genes in testis of diploid and tetraploid cyprinid fish

机译:二倍体和四倍体鲤类鱼类睾丸中精子运动相关基因的不同表达方式

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摘要

Sperm motility is an important standard to measure the fertility of male. In our previous study, we found that the diploid spermatozoa from allotetraploid hybrid (4nAT) had longer durations of rapid and slow progressive motility than haploid spermatozoa from common carp (COC). In this study, to explore sperm motility-related molecular mechanisms, we compared the testis tissues transcriptomes from 2-year-old male COC and 4nAT. The RNA-seq data revealed that 2985 genes were differentially expressed between COC and 4nAT, including 2216 upregulated and 769 downregulated genes in 4nAT. Some differentially expressed genes, such as tubulin genes, dynein, axonemal, heavy chain(dnah) genes, mitogen-activated protein kinase(mapk) genes, tektin 4, FOX transcription factors, proteasome genes, and ubiquitin carboxyl-terminal hydrolase(uchl) genes, are involved in the regulation of cell division, flagellar and ciliary motility, gene transcription, cytoskeleton, energy metabolism, and the ubiquitin–proteasome system, suggesting that these genes were related to sperm motility of the 4nAT. We confirmed the differential expression of 12 such genes in 4nAT by quantitative PCR. By western blotting, we also confirmed increased expression of Uchl3 in 4nAT testis. In addition, we identified 1915 and 2551 predicted long noncoding RNA (lncRNA) transcripts from testis tissue transcriptomes of COC and 4nAT, respectively. Of these, 1575 lncRNAs were specifically expressed in 4nAT and 939 were specifically expressed in COC. This study provides insights into the transcriptome profile of testis tissues from diploid and tetraploid, which are useful for research on regulatory mechanisms behind sperm motility in male polyploidy.
机译:精子活力是衡量男性生育能力的重要标准。在我们先前的研究中,我们发现异源四倍体杂种(4nAT)的二倍体精子比鲤鱼(COC)的单倍体精子具有更长的快速和缓慢的运动能力。在这项研究中,为了探索与精子运动相关的分子机制,我们比较了2岁男性COC和4nAT的睾丸组织转录组。 RNA-seq数据显示2985个基因在COC和4nAT之间差异表达,其中4nAT中有2216个上调基因和769个下调基因。一些差异表达的基因,例如微管蛋白基因,动力蛋白,轴突,重链(dnah)基因,促分裂原活化蛋白激酶(mapk)基因,tektin 4,FOX转录因子,蛋白酶体基因和泛素羧基末端水解酶(uchl)这些基因参与细胞分裂,鞭毛和纤毛运动,基因转录,细胞骨架,能量代谢和泛素-蛋白酶体系统的调控,表明这些基因与4nAT的精子运动有关。我们通过定量PCR证实了4nAT中12个此类基因的差异表达。通过蛋白质印迹,我们还证实了Uchl3在4nAT睾丸中的表达增加。此外,我们分别从COC和4nAT的睾丸组织转录组中鉴定出1915和2551个预测的长非编码RNA(lncRNA)转录本。其中,在4nAT中特异性表达1575个lncRNA,在COC中特异性表达939个。这项研究提供了从二倍体和四倍体睾丸组织的转录组概况的见解,这对于研究男性多倍体中精子运动的调控机制很有用。

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