{"doi":"10.1111/gtc.12086","title":"<scp>GATA</scp> factor switching from <scp>GATA</scp>2 to <scp>GATA</scp>1 contributes to erythroid differentiation","abstract":"<jats:p>Transcription factor <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>2 is highly expressed in hematopoietic stem cells and progenitors, whereas its expression declines after erythroid commitment of progenitors. In contrast, the start of <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1 expression coincides with the erythroid commitment and increases along with the erythroid differentiation. We refer this dynamic transition of <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content> factor expression to as the ‘<jats:styled-content style=\"fixed-case\">GATA</jats:styled-content> factor switching’. Here, we examined contribution of the <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content> factor switching to the erythroid differentiation. In <jats:italic>Gata1‐</jats:italic>knockdown embryos that concomitantly express <jats:styled-content style=\"fixed-case\"><jats:italic>Gata2</jats:italic></jats:styled-content>‐<jats:styled-content style=\"fixed-case\">GFP</jats:styled-content> reporter, high‐level expression of <jats:styled-content style=\"fixed-case\">GFP</jats:styled-content> reporter was detected in accumulated immature hematopoietic cells with impaired differentiation, demonstrating that <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1 represses <jats:styled-content style=\"fixed-case\"><jats:italic>Gata2</jats:italic></jats:styled-content> gene expression in hematopoietic progenitors <jats:italic>in vivo</jats:italic>. We have conducted chromatin immunoprecipitation (ChIP) on microarray analyses of <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>2 and <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1, and results indicate that the <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1‐binding sites widely overlap with the sites pre‐occupied by <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>2 before the <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1 expression. Importantly, erythroid genes harboring <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content> boxes bound by both <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1 and <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>2 tend to be expressed in immature erythroid cells, whereas those harboring <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content> boxes to which <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1 binds highly but <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>2 binds only weakly are important for the mature erythroid cell function. Our results thus support the contention that preceding binding of <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>2 helps the following binding of <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1 and thereby secures smooth expression of the transient‐phase genes.</jats:p>","journal":"Genes to Cells","year":2013,"id":659536,"datarank":0.6663976884735476,"base_score":4.442651256490317,"endowment":4.442651256490317,"self_citation_contribution":0.6663976884735476,"citation_network_contribution":0.0,"self_endowment_contribution":0.6663976884735476,"citer_contribution":0.0,"corpus_percentile":null,"corpus_rank":null,"citation_count":84,"citer_count":0,"citers_with_citation_signal":0,"citers_with_endowment":0,"datacite_reuse_total":0,"is_dataset":false,"is_dataset_confidence":null,"is_data_producer":false,"deposit_databanks":null,"is_oa":false,"file_count":0,"downloads":0,"has_version_chain":false,"published_date":null,"fair_score":null,"fair_percentile":null,"algorithm_id":"datarank_citation_only_1hop_v6","ranking_scope":"data_only","authors":[{"id":1721688,"name":"Maki Kobayashi‐Osaki","orcid":null,"position":1,"is_corresponding":false},{"id":1721690,"name":"Shuichi Tsutsumi","orcid":null,"position":2,"is_corresponding":false},{"id":898542,"name":"Xiaoqing Pan","orcid":"0000-0002-3559-5337","position":3,"is_corresponding":false},{"id":1721691,"name":"Shin'ya Ohmori","orcid":null,"position":4,"is_corresponding":false},{"id":77760,"name":"Jun Takai","orcid":null,"position":5,"is_corresponding":false},{"id":1477198,"name":"Takashi Moriguchi","orcid":"0000-0002-5341-8932","position":6,"is_corresponding":false},{"id":1721694,"name":"Osamu Ohneda","orcid":null,"position":7,"is_corresponding":false},{"id":1721695,"name":"Kinuko Ohneda","orcid":null,"position":8,"is_corresponding":false},{"id":1721696,"name":"Ritsuko Shimizu","orcid":null,"position":9,"is_corresponding":false},{"id":1721697,"name":"Yasuharu Kanki","orcid":null,"position":10,"is_corresponding":false},{"id":1050935,"name":"Tatsuhiko Kodama","orcid":"0000-0003-3747-7956","position":11,"is_corresponding":false},{"id":13188,"name":"Hiroyuki Aburatani","orcid":"0000-0003-0438-1544","position":12,"is_corresponding":false},{"id":19758,"name":"Masayuki Yamamoto","orcid":"0000-0002-9073-9436","position":13,"is_corresponding":false},{"id":1721687,"name":"Mikiko Suzuki","orcid":null,"position":0,"is_corresponding":false}],"reference_count":0,"raw_metadata":{"has_enrichment":true,"resolved":true,"title":"<scp>GATA</scp> factor switching from <scp>GATA</scp>2 to <scp>GATA</scp>1 contributes to erythroid differentiation","abstract":"<jats:p>Transcription factor <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>2 is highly expressed in hematopoietic stem cells and progenitors, whereas its expression declines after erythroid commitment of progenitors. In contrast, the start of <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1 expression coincides with the erythroid commitment and increases along with the erythroid differentiation. We refer this dynamic transition of <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content> factor expression to as the ‘<jats:styled-content style=\"fixed-case\">GATA</jats:styled-content> factor switching’. Here, we examined contribution of the <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content> factor switching to the erythroid differentiation. In <jats:italic>Gata1‐</jats:italic>knockdown embryos that concomitantly express <jats:styled-content style=\"fixed-case\"><jats:italic>Gata2</jats:italic></jats:styled-content>‐<jats:styled-content style=\"fixed-case\">GFP</jats:styled-content> reporter, high‐level expression of <jats:styled-content style=\"fixed-case\">GFP</jats:styled-content> reporter was detected in accumulated immature hematopoietic cells with impaired differentiation, demonstrating that <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1 represses <jats:styled-content style=\"fixed-case\"><jats:italic>Gata2</jats:italic></jats:styled-content> gene expression in hematopoietic progenitors <jats:italic>in vivo</jats:italic>. We have conducted chromatin immunoprecipitation (ChIP) on microarray analyses of <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>2 and <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1, and results indicate that the <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1‐binding sites widely overlap with the sites pre‐occupied by <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>2 before the <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1 expression. Importantly, erythroid genes harboring <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content> boxes bound by both <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1 and <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>2 tend to be expressed in immature erythroid cells, whereas those harboring <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content> boxes to which <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1 binds highly but <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>2 binds only weakly are important for the mature erythroid cell function. Our results thus support the contention that preceding binding of <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>2 helps the following binding of <jats:styled-content style=\"fixed-case\">GATA</jats:styled-content>1 and thereby secures smooth expression of the transient‐phase genes.</jats:p>","is_dataset_classified":null,"base_score":4.442651256490317,"endowment":4.442651256490317,"datacite_reuse_total":0,"file_count":0,"downloads":0,"views":0,"has_version_chain":false,"is_dataset":false,"is_oa":false,"pmid":"23911012","pmcid":null,"openalex_id":"https://openalex.org/W2049117415","authors":[],"funders":[],"total_grants":0,"fwci":2.4769,"citation_percentile":0.89430054,"influential_citations":0,"citation_trend":[{"year":2014,"count":9},{"year":2015,"count":5},{"year":2016,"count":4},{"year":2017,"count":11},{"year":2018,"count":5},{"year":2019,"count":4},{"year":2020,"count":7},{"year":2021,"count":8},{"year":2022,"count":6},{"year":2023,"count":4},{"year":2024,"count":6},{"year":2025,"count":9},{"year":2026,"count":6}],"oa_status":"bronze","license":"http://onlinelibrary.wiley.com/termsAndConditions#vor","oa_locations":[{"url":"https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/gtc.12086","host_type":"journal"},{"url":"https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/gtc.12086","host_type":"publisher"},{"url":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fgtc.12086","host_type":"publisher"},{"url":"https://onlinelibrary.wiley.com/doi/pdf/10.1111/gtc.12086","host_type":"publisher"},{"url":"https://doi.org/10.1111/gtc.12086","host_type":"journal"},{"url":"https://pubmed.ncbi.nlm.nih.gov/23911012","host_type":"repository"}],"fields_of_study":["Epigenetics and DNA Methylation","Acute Myeloid Leukemia Research","Hemoglobinopathies and Related Disorders","Animals","Binding Sites","Cell Differentiation","Erythroid Cells","Erythropoiesis","GATA1 Transcription Factor","GATA2 Transcription Factor","Gene Expression Regulation, Developmental","Hematopoietic Stem Cells","Mice","Mice, Transgenic"],"mesh_terms":["Animals","Binding Sites","Cell Differentiation","Erythropoiesis","Hematopoietic Stem Cells","Mice, Transgenic","Gene Expression Regulation, Developmental","Erythroid Cells","GATA1 Transcription Factor","GATA2 Transcription Factor","Mice"],"keywords":["GATA2","GATA1","GATA transcription factor","Transcription factor","Biology","Haematopoiesis","Gene knockdown","Cell biology","Cellular differentiation","Molecular biology","Gene expression","Stem cell","Genetics","Gene","Promoter"],"sdg_mappings":[],"linked_datasets":[],"clinical_trials":[],"software_tools":[],"database_accessions":[],"source":"live","citation_network_status":"fetched"},"created_at":"2026-08-12T07:06:48.713067Z","pmid":null,"pmcid":null,"fwci":null,"citation_percentile":null,"influential_citations":0,"oa_status":null,"license":null,"views":0,"total_file_size_bytes":0,"version_count":0,"fair_f":null,"fair_a":null,"fair_i":null,"fair_r":null,"fair_zscore":null,"fair_rationale":null,"fair_model":null,"fair_agent_version":null,"fair_fulltext_source":null,"fair_has_llm":null,"fair_computed_at":null,"clinical_trials":[],"software_tools":[],"db_accessions":[],"linked_datasets":[],"topics":[]}