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Genome-wide analysis of citrus TCP transcription factors and their responses to abiotic stresses
Citrus is one of the most important fruit crops in the world, and it is worthy to conduct more research on artificially controlling citrus plant growth and development to adapt to different cultivation patterns and environmental conditions. The plant-specific TEOSINTE BRANCHED1, CYCOLOIDEA, and PROL...
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Published in: | BMC plant biology 2022-07, Vol.22 (1), p.1-325, Article 325 |
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description | Citrus is one of the most important fruit crops in the world, and it is worthy to conduct more research on artificially controlling citrus plant growth and development to adapt to different cultivation patterns and environmental conditions. The plant-specific TEOSINTE BRANCHED1, CYCOLOIDEA, and PROLIFERATING CELL FACTORS (TCP) transcription factors are crucial regulators controlling plant growth and development, as well as responding to abiotic stresses. However, the information about citrus TCP transcription factors remains unclear. In this study, twenty putative TCP genes (CsTCPs) with the TCP domain were explored from Citrus sinensis genome, of which eleven (CsTCP3, - 4, - 5, - 6, - 10, - 11, - 15, - 16, - 18, - 19, - 20), five (CsTCP1, - 2, - 7, - 9, - 13), and four genes (CsTCP8, - 12, - 14, - 17) were unevenly distributed on chromosomes and divided into three subclades. Cis-acting element analysis indicated that most CsTCPs contained many phytohormone- and environment-responsive elements in promoter regions. All of CsTCPs were predominantly expressed in vegetative tissues or organs (stem, leaf, thorn, and bud) instead of reproductive tissues or organs (flower, fruit, and seed). Combined with collinearity analysis, CsTCP3, CsTCP9, and CsTCP13 may take part in leaf development; CsTCP12 and CsTCP14 may function in shoot branching, leaf development, or thorn development; CsTCP15 may participate in the development of stem, leaf, or thorn. In mature leaf, transcript levels of two CsTCPs (CsTCP19, - 20) were significantly increased while transcript levels of eight CsTCPs (CsTCP2, - 5, - 6, - 7, - 8, - 9, - 10, - 13) were significantly decreased by shading; except for two CsTCPs (CsTCP11, - 19), CsTCPs' transcript levels were significantly influenced by low temperature; moreover, transcript levels of two CsTCPs (CsTCP11, - 12) were significantly increased while five CsTCPs' (CsTCP14, - 16, - 18, - 19, - 20) transcript levels were significantly reduced by drought. This study provides significant clues for research on roles of CsTCPs in regulating citrus plant growth and development, as well as responding to abiotic stresses. |
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The plant-specific TEOSINTE BRANCHED1, CYCOLOIDEA, and PROLIFERATING CELL FACTORS (TCP) transcription factors are crucial regulators controlling plant growth and development, as well as responding to abiotic stresses. However, the information about citrus TCP transcription factors remains unclear. In this study, twenty putative TCP genes (CsTCPs) with the TCP domain were explored from Citrus sinensis genome, of which eleven (CsTCP3, - 4, - 5, - 6, - 10, - 11, - 15, - 16, - 18, - 19, - 20), five (CsTCP1, - 2, - 7, - 9, - 13), and four genes (CsTCP8, - 12, - 14, - 17) were unevenly distributed on chromosomes and divided into three subclades. Cis-acting element analysis indicated that most CsTCPs contained many phytohormone- and environment-responsive elements in promoter regions. All of CsTCPs were predominantly expressed in vegetative tissues or organs (stem, leaf, thorn, and bud) instead of reproductive tissues or organs (flower, fruit, and seed). Combined with collinearity analysis, CsTCP3, CsTCP9, and CsTCP13 may take part in leaf development; CsTCP12 and CsTCP14 may function in shoot branching, leaf development, or thorn development; CsTCP15 may participate in the development of stem, leaf, or thorn. In mature leaf, transcript levels of two CsTCPs (CsTCP19, - 20) were significantly increased while transcript levels of eight CsTCPs (CsTCP2, - 5, - 6, - 7, - 8, - 9, - 10, - 13) were significantly decreased by shading; except for two CsTCPs (CsTCP11, - 19), CsTCPs' transcript levels were significantly influenced by low temperature; moreover, transcript levels of two CsTCPs (CsTCP11, - 12) were significantly increased while five CsTCPs' (CsTCP14, - 16, - 18, - 19, - 20) transcript levels were significantly reduced by drought. This study provides significant clues for research on roles of CsTCPs in regulating citrus plant growth and development, as well as responding to abiotic stresses.</description><identifier>ISSN: 1471-2229</identifier><identifier>EISSN: 1471-2229</identifier><identifier>DOI: 10.1186/s12870-022-03709-3</identifier><identifier>PMID: 35790897</identifier><language>eng</language><publisher>London: BioMed Central Ltd</publisher><subject>Abiotic stress ; Agricultural research ; Amino acids ; Binding sites ; Chromosomes ; Citrus ; Citrus fruits ; Citrus sinensis ; Collinearity ; Drought ; Environmental conditions ; Expression pattern ; Fruit crops ; Fruits ; Gene expression ; Genes ; Genetic aspects ; Genome-wide analysis ; Genomes ; Hardiness ; Leaves ; Low temperature ; Organs ; Physiological aspects ; Plant growth ; Plant hormones ; Plants ; Proteins ; Stems ; Stresses ; TCP family ; Transcription factors</subject><ispartof>BMC plant biology, 2022-07, Vol.22 (1), p.1-325, Article 325</ispartof><rights>COPYRIGHT 2022 BioMed Central Ltd.</rights><rights>2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c574t-a056978c812367a7fb873b8cc8aaa7af8dc895fd7bc1dc3929b83695133ed5e43</citedby><cites>FETCH-LOGICAL-c574t-a056978c812367a7fb873b8cc8aaa7af8dc895fd7bc1dc3929b83695133ed5e43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258177/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2691569828?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids></links><search><creatorcontrib>Liu, Dong-Hai</creatorcontrib><creatorcontrib>Luo, Yin</creatorcontrib><creatorcontrib>Han, Han</creatorcontrib><creatorcontrib>Liu, Yong-Zhong</creatorcontrib><creatorcontrib>Alam, Shariq Mahmood</creatorcontrib><creatorcontrib>Zhao, Hui-Xing</creatorcontrib><creatorcontrib>Li, Yan-Ting</creatorcontrib><title>Genome-wide analysis of citrus TCP transcription factors and their responses to abiotic stresses</title><title>BMC plant biology</title><description>Citrus is one of the most important fruit crops in the world, and it is worthy to conduct more research on artificially controlling citrus plant growth and development to adapt to different cultivation patterns and environmental conditions. The plant-specific TEOSINTE BRANCHED1, CYCOLOIDEA, and PROLIFERATING CELL FACTORS (TCP) transcription factors are crucial regulators controlling plant growth and development, as well as responding to abiotic stresses. However, the information about citrus TCP transcription factors remains unclear. In this study, twenty putative TCP genes (CsTCPs) with the TCP domain were explored from Citrus sinensis genome, of which eleven (CsTCP3, - 4, - 5, - 6, - 10, - 11, - 15, - 16, - 18, - 19, - 20), five (CsTCP1, - 2, - 7, - 9, - 13), and four genes (CsTCP8, - 12, - 14, - 17) were unevenly distributed on chromosomes and divided into three subclades. Cis-acting element analysis indicated that most CsTCPs contained many phytohormone- and environment-responsive elements in promoter regions. All of CsTCPs were predominantly expressed in vegetative tissues or organs (stem, leaf, thorn, and bud) instead of reproductive tissues or organs (flower, fruit, and seed). Combined with collinearity analysis, CsTCP3, CsTCP9, and CsTCP13 may take part in leaf development; CsTCP12 and CsTCP14 may function in shoot branching, leaf development, or thorn development; CsTCP15 may participate in the development of stem, leaf, or thorn. In mature leaf, transcript levels of two CsTCPs (CsTCP19, - 20) were significantly increased while transcript levels of eight CsTCPs (CsTCP2, - 5, - 6, - 7, - 8, - 9, - 10, - 13) were significantly decreased by shading; except for two CsTCPs (CsTCP11, - 19), CsTCPs' transcript levels were significantly influenced by low temperature; moreover, transcript levels of two CsTCPs (CsTCP11, - 12) were significantly increased while five CsTCPs' (CsTCP14, - 16, - 18, - 19, - 20) transcript levels were significantly reduced by drought. This study provides significant clues for research on roles of CsTCPs in regulating citrus plant growth and development, as well as responding to abiotic stresses.</description><subject>Abiotic stress</subject><subject>Agricultural research</subject><subject>Amino acids</subject><subject>Binding sites</subject><subject>Chromosomes</subject><subject>Citrus</subject><subject>Citrus fruits</subject><subject>Citrus sinensis</subject><subject>Collinearity</subject><subject>Drought</subject><subject>Environmental conditions</subject><subject>Expression pattern</subject><subject>Fruit crops</subject><subject>Fruits</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genome-wide analysis</subject><subject>Genomes</subject><subject>Hardiness</subject><subject>Leaves</subject><subject>Low temperature</subject><subject>Organs</subject><subject>Physiological aspects</subject><subject>Plant growth</subject><subject>Plant hormones</subject><subject>Plants</subject><subject>Proteins</subject><subject>Stems</subject><subject>Stresses</subject><subject>TCP family</subject><subject>Transcription factors</subject><issn>1471-2229</issn><issn>1471-2229</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkl1vFCEUhidGY2v1D3hF4o1eTOVrBrgxaTZaN2mi0XqNZ_jYspkdVmDU_nvZbqOOMYRADs95gXPepnlO8Dkhsn-dCZUCt5jSFjOBVcseNKeEC9JSStXDv_YnzZOctxgTIbl63JywTigslThtvl66Ke5c-yNYh2CC8TaHjKJHJpQ0Z3S9-ohKgimbFPYlxAl5MCWmXGGLyo0LCSWX93HKLqMSEQwhlmBQLjVcY0-bRx7G7J7dr2fNl3dvr1fv26sPl-vVxVVrOsFLC7jrlZBGEsp6AcIPUrBBGiMBQICX1kjVeSsGQ6xhiqpBsl51hDFnO8fZWbM-6toIW71PYQfpVkcI-i4Q00ZDqg8bnSZVc7BCEMwJl7SDvhs8EIqpJ9YOtmq9OWrt52HnrHFTLcG4EF2eTOFGb-J3rWgniRBV4OW9QIrfZpeL3oVs3DjC5OKcNe1lxzmvs6Iv_kG3cU61EQdKkVoVSeUfagP1A2Hysd5rDqL6onaeUYn5gTr_D1WHdbtg4uR8qPFFwqtFQmWK-1k2MOes158_LVl6ZE2KOSfnf9eDYH3woz76UVc_6js_asZ-Af1g0Iw</recordid><startdate>20220706</startdate><enddate>20220706</enddate><creator>Liu, Dong-Hai</creator><creator>Luo, Yin</creator><creator>Han, Han</creator><creator>Liu, Yong-Zhong</creator><creator>Alam, Shariq Mahmood</creator><creator>Zhao, Hui-Xing</creator><creator>Li, Yan-Ting</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20220706</creationdate><title>Genome-wide analysis of citrus TCP transcription factors and their responses to abiotic stresses</title><author>Liu, Dong-Hai ; Luo, Yin ; Han, Han ; Liu, Yong-Zhong ; Alam, Shariq Mahmood ; Zhao, Hui-Xing ; Li, Yan-Ting</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c574t-a056978c812367a7fb873b8cc8aaa7af8dc895fd7bc1dc3929b83695133ed5e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Abiotic stress</topic><topic>Agricultural research</topic><topic>Amino acids</topic><topic>Binding sites</topic><topic>Chromosomes</topic><topic>Citrus</topic><topic>Citrus fruits</topic><topic>Citrus sinensis</topic><topic>Collinearity</topic><topic>Drought</topic><topic>Environmental conditions</topic><topic>Expression pattern</topic><topic>Fruit crops</topic><topic>Fruits</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genome-wide analysis</topic><topic>Genomes</topic><topic>Hardiness</topic><topic>Leaves</topic><topic>Low temperature</topic><topic>Organs</topic><topic>Physiological aspects</topic><topic>Plant growth</topic><topic>Plant hormones</topic><topic>Plants</topic><topic>Proteins</topic><topic>Stems</topic><topic>Stresses</topic><topic>TCP family</topic><topic>Transcription factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Dong-Hai</creatorcontrib><creatorcontrib>Luo, Yin</creatorcontrib><creatorcontrib>Han, Han</creatorcontrib><creatorcontrib>Liu, Yong-Zhong</creatorcontrib><creatorcontrib>Alam, Shariq Mahmood</creatorcontrib><creatorcontrib>Zhao, Hui-Xing</creatorcontrib><creatorcontrib>Li, Yan-Ting</creatorcontrib><collection>CrossRef</collection><collection>Science (Gale in Context)</collection><collection>ProQuest Central (Corporate)</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMC plant biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Dong-Hai</au><au>Luo, Yin</au><au>Han, Han</au><au>Liu, Yong-Zhong</au><au>Alam, Shariq Mahmood</au><au>Zhao, Hui-Xing</au><au>Li, Yan-Ting</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genome-wide analysis of citrus TCP transcription factors and their responses to abiotic stresses</atitle><jtitle>BMC plant biology</jtitle><date>2022-07-06</date><risdate>2022</risdate><volume>22</volume><issue>1</issue><spage>1</spage><epage>325</epage><pages>1-325</pages><artnum>325</artnum><issn>1471-2229</issn><eissn>1471-2229</eissn><abstract>Citrus is one of the most important fruit crops in the world, and it is worthy to conduct more research on artificially controlling citrus plant growth and development to adapt to different cultivation patterns and environmental conditions. The plant-specific TEOSINTE BRANCHED1, CYCOLOIDEA, and PROLIFERATING CELL FACTORS (TCP) transcription factors are crucial regulators controlling plant growth and development, as well as responding to abiotic stresses. However, the information about citrus TCP transcription factors remains unclear. In this study, twenty putative TCP genes (CsTCPs) with the TCP domain were explored from Citrus sinensis genome, of which eleven (CsTCP3, - 4, - 5, - 6, - 10, - 11, - 15, - 16, - 18, - 19, - 20), five (CsTCP1, - 2, - 7, - 9, - 13), and four genes (CsTCP8, - 12, - 14, - 17) were unevenly distributed on chromosomes and divided into three subclades. Cis-acting element analysis indicated that most CsTCPs contained many phytohormone- and environment-responsive elements in promoter regions. All of CsTCPs were predominantly expressed in vegetative tissues or organs (stem, leaf, thorn, and bud) instead of reproductive tissues or organs (flower, fruit, and seed). Combined with collinearity analysis, CsTCP3, CsTCP9, and CsTCP13 may take part in leaf development; CsTCP12 and CsTCP14 may function in shoot branching, leaf development, or thorn development; CsTCP15 may participate in the development of stem, leaf, or thorn. In mature leaf, transcript levels of two CsTCPs (CsTCP19, - 20) were significantly increased while transcript levels of eight CsTCPs (CsTCP2, - 5, - 6, - 7, - 8, - 9, - 10, - 13) were significantly decreased by shading; except for two CsTCPs (CsTCP11, - 19), CsTCPs' transcript levels were significantly influenced by low temperature; moreover, transcript levels of two CsTCPs (CsTCP11, - 12) were significantly increased while five CsTCPs' (CsTCP14, - 16, - 18, - 19, - 20) transcript levels were significantly reduced by drought. This study provides significant clues for research on roles of CsTCPs in regulating citrus plant growth and development, as well as responding to abiotic stresses.</abstract><cop>London</cop><pub>BioMed Central Ltd</pub><pmid>35790897</pmid><doi>10.1186/s12870-022-03709-3</doi><oa>free_for_read</oa></addata></record> |
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subjects | Abiotic stress Agricultural research Amino acids Binding sites Chromosomes Citrus Citrus fruits Citrus sinensis Collinearity Drought Environmental conditions Expression pattern Fruit crops Fruits Gene expression Genes Genetic aspects Genome-wide analysis Genomes Hardiness Leaves Low temperature Organs Physiological aspects Plant growth Plant hormones Plants Proteins Stems Stresses TCP family Transcription factors |
title | Genome-wide analysis of citrus TCP transcription factors and their responses to abiotic stresses |
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