Single-nucleus transcriptomes reveal evolutionary and functional properties of cell types in the Drosophila accessory gland.
Single-nucleus transcriptomes reveal evolutionary and functional properties of cell types in the Drosophila accessory gland.
复制标题
单核转录组揭示了果蝇副腺细胞类型的进化和功能特性。
DOI:
10.1093/genetics/iyab213
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发表时间:
2022
期刊:
影响因子:
3.3
通讯作者:
Begun,DavidJ
中科院分区:
文献类型:
--
作者:
Majane,AlexC;Cridland,JulieM;Begun,DavidJ
Many traits responsible for male reproduction evolve quickly, including gene expression phenotypes in germline and somatic male reproductive tissues. Rapid male evolution in polyandrous species is thought to be driven by competition among males for fertilizations and conflicts between male and female fitness interests that manifest in postcopulatory phenotypes. InDrosophila, seminal fluid proteins secreted by three major cell types of the male accessory gland and ejaculatory duct are required for female sperm storage and use, and influence female postcopulatory traits. Recent work has shown that these cell types have overlapping but distinct effects on female postcopulatory biology, yet relatively little is known about their evolutionary properties. Here, we use single-nucleus RNA-Seq of the accessory gland and ejaculatory duct fromDrosophila melanogasterand two closely related species to comprehensively describe the cell diversity of these tissues and their transcriptome evolution for the first time. We find that seminal fluid transcripts are strongly partitioned across the major cell types, and expression of many other genes additionally defines each cell type. We also report previously undocumented diversity in main cells. Transcriptome divergence was found to be heterogeneous across cell types and lineages, revealing a complex evolutionary process. Furthermore, protein adaptation varied across cell types, with potential consequences for our understanding of selection on male postcopulatory traits.
影响因子:
--
作者:
M. Campanacci;M. Laus
通讯作者:
M. Laus
影响因子:
4.2
作者:
J. Johnston;T. Harries;C. E. Alexander;A. Alexander
通讯作者:
A. Alexander