{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,28]],"date-time":"2026-02-28T08:47:05Z","timestamp":1772268425592,"version":"3.50.1"},"reference-count":57,"publisher":"PeerJ","license":[{"start":{"date-parts":[[2023,1,9]],"date-time":"2023-01-09T00:00:00Z","timestamp":1673222400000},"content-version":"unspecified","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"name":"The RFBR","award":["Project No. 20-04-00496-a"],"award-info":[{"award-number":["Project No. 20-04-00496-a"]}]},{"name":"The Ministry of Science and Higher Education of the Russian Federation","award":["Project No. FWNR-2022-0015"],"award-info":[{"award-number":["Project No. FWNR-2022-0015"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"abstract":"<jats:p>\n                    The GAGA protein (also known as GAF) is a transcription factor encoded by the\n                    <jats:italic>Trl<\/jats:italic>\n                    gene in\n                    <jats:italic>D. melanogaster<\/jats:italic>\n                    . GAGA is involved in the regulation of transcription of many genes at all stages of fly development and life. Recently, we investigated the participation of GAGA in spermatogenesis and discovered that\n                    <jats:italic>Trl<\/jats:italic>\n                    mutants experience massive degradation of germline cells in the testes.\n                    <jats:italic>Trl<\/jats:italic>\n                    underexpression induces autophagic death of spermatocytes, thereby leading to reduced testis size. Here, we aimed to determine the role of the transcription factor GAGA in the regulation of ectopic germline cell death. We investigated how\n                    <jats:italic>Trl<\/jats:italic>\n                    underexpression affects gene expression in the testes. We identified 15,993 genes in three biological replicates of our RNA-seq analysis and compared transcript levels between hypomorphic\n                    <jats:italic>Trl<\/jats:italic>\n                    <jats:sup>R85<\/jats:sup>\n                    \/\n                    <jats:italic>Trl<\/jats:italic>\n                    <jats:sup>362<\/jats:sup>\n                    and\n                    <jats:italic>Oregon<\/jats:italic>\n                    testes. A total of 2,437 differentially expressed genes were found, including 1,686 upregulated and 751 downregulated genes. At the transcriptional level, we detected the development of cellular stress in the\n                    <jats:italic>Trl<\/jats:italic>\n                    -mutant testes: downregulation of the genes normally expressed in the testes (indicating slowed or abrogated spermatocyte differentiation) and increased expression of metabolic and proteolysis-related genes, including stress response long noncoding RNAs. Nonetheless, in the Flybase Gene Ontology lists of genes related to cell death, autophagy, or stress, there was no enrichment with GAGA-binding sites. Furthermore, we did not identify any specific GAGA-dependent cell death pathway that could regulate spermatocyte death. Thus, our data suggest that GAGA deficiency in male germline cells leads to an imbalance of metabolic processes, impaired mitochondrial function, and cell death due to cellular stress.\n                  <\/jats:p>","DOI":"10.7717\/peerj.14063","type":"journal-article","created":{"date-parts":[[2023,1,9]],"date-time":"2023-01-09T03:48:34Z","timestamp":1673236114000},"page":"e14063","source":"Crossref","is-referenced-by-count":1,"title":["The complex role of transcription factor GAGA in germline death during\n                    <i>Drosophila<\/i>\n                    spermatogenesis: transcriptomic and bioinformatic analyses"],"prefix":"10.7717","volume":"11","author":[{"given":"Svetlana","family":"Fedorova","sequence":"first","affiliation":[{"name":"Department of Cell Biology, Institute of Cytology and Genetics SB RAS, Novosibirsk, Russian Federation"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Natalya V.","family":"Dorogova","sequence":"additional","affiliation":[{"name":"Department of Cell Biology, Institute of Cytology and Genetics SB RAS, Novosibirsk, Russian Federation"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dmitriy A.","family":"Karagodin","sequence":"additional","affiliation":[{"name":"Department of Cell Biology, Institute of Cytology and Genetics SB RAS, Novosibirsk, Russian Federation"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Dmitry Yu","family":"Oshchepkov","sequence":"additional","affiliation":[{"name":"Department of Systems Biology, Institute of Cytology and Genetics SB RAS, Novosibirsk, Russian Federation"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ilya I.","family":"Brusentsov","sequence":"additional","affiliation":[{"name":"Department of Cell Biology, Institute of Cytology and Genetics SB RAS, Novosibirsk, Russian Federation"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Natalya 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