<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chen X</submitter><funding>Research Project of Nantong Health Commission</funding><funding>the Nantong Key Young Medical Talent Program</funding><funding>Workstation of Academician Liu Yixun</funding><funding>Basic Science Research Program of Nantong City</funding><funding>the Fund of Xuzhou Science and Technology</funding><funding>Jiangsu province senile health scientific research project</funding><funding>Science and Technology Project of Nantong City</funding><funding>National Natural Science Foundation of China</funding><funding>Xuzhou Pengcheng Talents - Medical Young Reserve Talents</funding><funding>the Open Fund of Jiangsu Key Laboratory for New Drug Research and Clinical Pharmacy</funding><funding>Natural Science Foundation of Jiangsu Province</funding><pagination>e14057</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10928582</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(3)</volume><pubmed_abstract>Aging is a complex biological process leading to impaired functions, with a variety of hallmarks. In the testis of Drosophila, the terminal epithelium region is involved in spermatid release and maturation, while its functional diversity and regulatory mechanism remain poorly understood. In this study, we performed single-cell RNA-sequencing analysis (scRNA-seq) to characterize the transcriptomes of terminal epithelium in Drosophila testes at 2-, 10 and 40-Days. Terminal epithelium populations were defined with Metallothionein A (MtnA) and subdivided into six novel sub-cell clusters (EP0-EP5), and a series of marker genes were identified based on their expressions. The data revealed the functional characteristics of terminal epithelium populations, such as tight junction, focal adhesion, b</pubmed_abstract><journal>Aging cell</journal><pubmed_title>Single-cell transcriptome characteristics of testicular terminal epithelium lineages during aging in the Drosophila.</pubmed_title><pmcid>PMC10928582</pmcid><funding_grant_id>XWRCSL20220162</funding_grant_id><funding_grant_id>QA2021016</funding_grant_id><funding_grant_id>BK20221376</funding_grant_id><funding_grant_id>JC12022006</funding_grant_id><funding_grant_id>LR2021035</funding_grant_id><funding_grant_id>2-2018.11.1</funding_grant_id><funding_grant_id>82101891</funding_grant_id><funding_grant_id>KC20092</funding_grant_id><funding_grant_id>JC2021119</funding_grant_id><funding_grant_id>82071838</funding_grant_id><pubmed_authors>Zheng Y</pubmed_authors><pubmed_authors>Sun C</pubmed_authors><pubmed_authors>Ji L</pubmed_authors><pubmed_authors>Zheng S</pubmed_authors><pubmed_authors>Gu Z</pubmed_authors><pubmed_authors>Huang Q</pubmed_authors><pubmed_authors>Yu J</pubmed_authors><pubmed_authors>Cheng X</pubmed_authors><pubmed_authors>Shi Y</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Qi Y</pubmed_authors><pubmed_authors>Cao Y</pubmed_authors><pubmed_authors>Chen X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-cell transcriptome characteristics of testicular terminal epithelium lineages during aging in the Drosophila.</name><description>Aging is a complex biological process leading to impaired functions, with a variety of hallmarks. In the testis of Drosophila, the terminal epithelium region is involved in spermatid release and maturation, while its functional diversity and regulatory mechanism remain poorly understood. In this study, we performed single-cell RNA-sequencing analysis (scRNA-seq) to characterize the transcriptomes of terminal epithelium in Drosophila testes at 2-, 10 and 40-Days. Terminal epithelium populations were defined with Metallothionein A (MtnA) and subdivided into six novel sub-cell clusters (EP0-EP5), and a series of marker genes were identified based on their expressions. The data revealed the functional characteristics of terminal epithelium populations, such as tight junction, focal adhesion, b</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-07-14T22:09:58.35Z</modification><creation>2025-04-04T21:30:55.737Z</creation></dates><accession>S-EPMC10928582</accession><cross_references><pubmed>38044573</pubmed><doi>10.1111/acel.14057</doi></cross_references></HashMap>