Identification and characterization of Rubisco activase genes in Oryza punctata
Rubisco activase (Rca), a specific chaperone, catalyzes the in vivo activation of Rubisco, and thus plays a major role in plant photosynthesis. Although the genes encoding Rubisco activase have been studied in many model or economic plants, few studies have analyzed their homologs in plants of close...
Gespeichert in:
Veröffentlicht in: | Journal of systematics and evolution : JSE 2017-05, Vol.55 (3), p.200-207 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 207 |
---|---|
container_issue | 3 |
container_start_page | 200 |
container_title | Journal of systematics and evolution : JSE |
container_volume | 55 |
creator | Xu, Si Qin, Zong‐Yan Gong, Pi‐Chang Dong, Qian‐Li Bao, Ying |
description | Rubisco activase (Rca), a specific chaperone, catalyzes the in vivo activation of Rubisco, and thus plays a major role in plant photosynthesis. Although the genes encoding Rubisco activase have been studied in many model or economic plants, few studies have analyzed their homologs in plants of closely related crop species. In this study, an Rca gene was identified and characterized in a wild relative of rice, Oryza punctata Kotschy ex Steud. The gene was 2747 bp long and possessed six exons and five introns with 47% GC content. Furthermore, cDNA sequencing produced two transcripts, Real and RcaS, that differed in the sequence by an inclusion of 99 bp at the carboxy terminus of ReaL. Sequence comparison between the two transcripts and the genomic DNA showed that there was a 20-bp alternative splicing event that occurred at the fifth intron of the gene leading to the synthesis of a short polypeptide. The leaf transcriptome analysis showed that RcaS had a higher expression level than that of RcaL in a normal growth environment. In addition, the yeast two-hybrid assays showed the small isoform of Rubisco activase in close contact with the large subunit of the Rubisco in this species, supporting the side-on binding model of interaction between two proteins. This study broadens our understanding of the molecular characteristics of some essential genes in photosynthesis. |
doi_str_mv | 10.1111/jse.12242 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1897065898</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cqvip_id>672274893</cqvip_id><sourcerecordid>1897065898</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3242-826c8317194bdf20cbc5c3ce43a4b1934ff88ac42b4c09754025f8ea8283ca153</originalsourceid><addsrcrecordid>eNp1kE1PAjEQhhujiYge_AeNnjws9Gu37dEQVIwJiR_npltaKMEutIsGfr3VRW_OZSaT531n8gJwidEA5xoukx1gQhg5Aj3MS1lUguLjPFecFUxicQrOUloiVHHBqx6YTmY2tN55o1vfBKjDDJqFjtq0Nvp9t2wcfN7WPpkG5r3_0MnCuQ02QR_gNO72Gq63wbS61efgxOlVsheH3gdvd-PX0UPxNL2fjG6fCkPzc4UglcmPcSxZPXMEmdqUhhrLqGY1lpQ5J4Q2jNTMIMlLhkjphNWCCGo0LmkfXHe-69hstja1atlsY8gnFRaSo6oUUmTqpqNMbFKK1ql19O867hRG6jsvlfNSP3lldtixn35ld_-D6vFl_Ku4OrgvmjDf-DD_U1WcEM6EpPQLsXp3jw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1897065898</pqid></control><display><type>article</type><title>Identification and characterization of Rubisco activase genes in Oryza punctata</title><source>Wiley Online Library All Journals</source><creator>Xu, Si ; Qin, Zong‐Yan ; Gong, Pi‐Chang ; Dong, Qian‐Li ; Bao, Ying</creator><creatorcontrib>Xu, Si ; Qin, Zong‐Yan ; Gong, Pi‐Chang ; Dong, Qian‐Li ; Bao, Ying</creatorcontrib><description>Rubisco activase (Rca), a specific chaperone, catalyzes the in vivo activation of Rubisco, and thus plays a major role in plant photosynthesis. Although the genes encoding Rubisco activase have been studied in many model or economic plants, few studies have analyzed their homologs in plants of closely related crop species. In this study, an Rca gene was identified and characterized in a wild relative of rice, Oryza punctata Kotschy ex Steud. The gene was 2747 bp long and possessed six exons and five introns with 47% GC content. Furthermore, cDNA sequencing produced two transcripts, Real and RcaS, that differed in the sequence by an inclusion of 99 bp at the carboxy terminus of ReaL. Sequence comparison between the two transcripts and the genomic DNA showed that there was a 20-bp alternative splicing event that occurred at the fifth intron of the gene leading to the synthesis of a short polypeptide. The leaf transcriptome analysis showed that RcaS had a higher expression level than that of RcaL in a normal growth environment. In addition, the yeast two-hybrid assays showed the small isoform of Rubisco activase in close contact with the large subunit of the Rubisco in this species, supporting the side-on binding model of interaction between two proteins. This study broadens our understanding of the molecular characteristics of some essential genes in photosynthesis.</description><identifier>ISSN: 1674-4918</identifier><identifier>EISSN: 1759-6831</identifier><identifier>DOI: 10.1111/jse.12242</identifier><language>eng</language><publisher>Beijing: Wiley Subscription Services, Inc</publisher><subject>Alternative splicing ; cDNA测序 ; Deoxyribonucleic acid ; DNA ; Economic analysis ; Economic models ; Economic planning ; Exons ; expression divergence ; Gene expression ; Genes ; Homology ; Introns ; Nucleotide sequence ; Oryza ; Photosynthesis ; protein interaction ; Proteins ; Ribulose-bisphosphate carboxylase ; Rubisco activase ; Rubisco活化酶 ; Splicing ; wild rice ; Yeast ; 光合作用 ; 基因组DNA ; 经济植物 ; 酶基因 ; 鉴定</subject><ispartof>Journal of systematics and evolution : JSE, 2017-05, Vol.55 (3), p.200-207</ispartof><rights>2017 Institute of Botany, Chinese Academy of Sciences</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3242-826c8317194bdf20cbc5c3ce43a4b1934ff88ac42b4c09754025f8ea8283ca153</citedby><cites>FETCH-LOGICAL-c3242-826c8317194bdf20cbc5c3ce43a4b1934ff88ac42b4c09754025f8ea8283ca153</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/94666A/94666A.jpg</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjse.12242$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjse.12242$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27928,27929,45578,45579</link.rule.ids></links><search><creatorcontrib>Xu, Si</creatorcontrib><creatorcontrib>Qin, Zong‐Yan</creatorcontrib><creatorcontrib>Gong, Pi‐Chang</creatorcontrib><creatorcontrib>Dong, Qian‐Li</creatorcontrib><creatorcontrib>Bao, Ying</creatorcontrib><title>Identification and characterization of Rubisco activase genes in Oryza punctata</title><title>Journal of systematics and evolution : JSE</title><addtitle>Journal of Systematics and Evolution</addtitle><description>Rubisco activase (Rca), a specific chaperone, catalyzes the in vivo activation of Rubisco, and thus plays a major role in plant photosynthesis. Although the genes encoding Rubisco activase have been studied in many model or economic plants, few studies have analyzed their homologs in plants of closely related crop species. In this study, an Rca gene was identified and characterized in a wild relative of rice, Oryza punctata Kotschy ex Steud. The gene was 2747 bp long and possessed six exons and five introns with 47% GC content. Furthermore, cDNA sequencing produced two transcripts, Real and RcaS, that differed in the sequence by an inclusion of 99 bp at the carboxy terminus of ReaL. Sequence comparison between the two transcripts and the genomic DNA showed that there was a 20-bp alternative splicing event that occurred at the fifth intron of the gene leading to the synthesis of a short polypeptide. The leaf transcriptome analysis showed that RcaS had a higher expression level than that of RcaL in a normal growth environment. In addition, the yeast two-hybrid assays showed the small isoform of Rubisco activase in close contact with the large subunit of the Rubisco in this species, supporting the side-on binding model of interaction between two proteins. This study broadens our understanding of the molecular characteristics of some essential genes in photosynthesis.</description><subject>Alternative splicing</subject><subject>cDNA测序</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Economic analysis</subject><subject>Economic models</subject><subject>Economic planning</subject><subject>Exons</subject><subject>expression divergence</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Homology</subject><subject>Introns</subject><subject>Nucleotide sequence</subject><subject>Oryza</subject><subject>Photosynthesis</subject><subject>protein interaction</subject><subject>Proteins</subject><subject>Ribulose-bisphosphate carboxylase</subject><subject>Rubisco activase</subject><subject>Rubisco活化酶</subject><subject>Splicing</subject><subject>wild rice</subject><subject>Yeast</subject><subject>光合作用</subject><subject>基因组DNA</subject><subject>经济植物</subject><subject>酶基因</subject><subject>鉴定</subject><issn>1674-4918</issn><issn>1759-6831</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kE1PAjEQhhujiYge_AeNnjws9Gu37dEQVIwJiR_npltaKMEutIsGfr3VRW_OZSaT531n8gJwidEA5xoukx1gQhg5Aj3MS1lUguLjPFecFUxicQrOUloiVHHBqx6YTmY2tN55o1vfBKjDDJqFjtq0Nvp9t2wcfN7WPpkG5r3_0MnCuQ02QR_gNO72Gq63wbS61efgxOlVsheH3gdvd-PX0UPxNL2fjG6fCkPzc4UglcmPcSxZPXMEmdqUhhrLqGY1lpQ5J4Q2jNTMIMlLhkjphNWCCGo0LmkfXHe-69hstja1atlsY8gnFRaSo6oUUmTqpqNMbFKK1ql19O867hRG6jsvlfNSP3lldtixn35ld_-D6vFl_Ku4OrgvmjDf-DD_U1WcEM6EpPQLsXp3jw</recordid><startdate>201705</startdate><enddate>201705</enddate><creator>Xu, Si</creator><creator>Qin, Zong‐Yan</creator><creator>Gong, Pi‐Chang</creator><creator>Dong, Qian‐Li</creator><creator>Bao, Ying</creator><general>Wiley Subscription Services, Inc</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W94</scope><scope>WU4</scope><scope>~WA</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope></search><sort><creationdate>201705</creationdate><title>Identification and characterization of Rubisco activase genes in Oryza punctata</title><author>Xu, Si ; Qin, Zong‐Yan ; Gong, Pi‐Chang ; Dong, Qian‐Li ; Bao, Ying</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3242-826c8317194bdf20cbc5c3ce43a4b1934ff88ac42b4c09754025f8ea8283ca153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Alternative splicing</topic><topic>cDNA测序</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>Economic analysis</topic><topic>Economic models</topic><topic>Economic planning</topic><topic>Exons</topic><topic>expression divergence</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Homology</topic><topic>Introns</topic><topic>Nucleotide sequence</topic><topic>Oryza</topic><topic>Photosynthesis</topic><topic>protein interaction</topic><topic>Proteins</topic><topic>Ribulose-bisphosphate carboxylase</topic><topic>Rubisco activase</topic><topic>Rubisco活化酶</topic><topic>Splicing</topic><topic>wild rice</topic><topic>Yeast</topic><topic>光合作用</topic><topic>基因组DNA</topic><topic>经济植物</topic><topic>酶基因</topic><topic>鉴定</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Si</creatorcontrib><creatorcontrib>Qin, Zong‐Yan</creatorcontrib><creatorcontrib>Gong, Pi‐Chang</creatorcontrib><creatorcontrib>Dong, Qian‐Li</creatorcontrib><creatorcontrib>Bao, Ying</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-自然科学</collection><collection>中文科技期刊数据库-自然科学-生物科学</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><jtitle>Journal of systematics and evolution : JSE</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Si</au><au>Qin, Zong‐Yan</au><au>Gong, Pi‐Chang</au><au>Dong, Qian‐Li</au><au>Bao, Ying</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification and characterization of Rubisco activase genes in Oryza punctata</atitle><jtitle>Journal of systematics and evolution : JSE</jtitle><addtitle>Journal of Systematics and Evolution</addtitle><date>2017-05</date><risdate>2017</risdate><volume>55</volume><issue>3</issue><spage>200</spage><epage>207</epage><pages>200-207</pages><issn>1674-4918</issn><eissn>1759-6831</eissn><abstract>Rubisco activase (Rca), a specific chaperone, catalyzes the in vivo activation of Rubisco, and thus plays a major role in plant photosynthesis. Although the genes encoding Rubisco activase have been studied in many model or economic plants, few studies have analyzed their homologs in plants of closely related crop species. In this study, an Rca gene was identified and characterized in a wild relative of rice, Oryza punctata Kotschy ex Steud. The gene was 2747 bp long and possessed six exons and five introns with 47% GC content. Furthermore, cDNA sequencing produced two transcripts, Real and RcaS, that differed in the sequence by an inclusion of 99 bp at the carboxy terminus of ReaL. Sequence comparison between the two transcripts and the genomic DNA showed that there was a 20-bp alternative splicing event that occurred at the fifth intron of the gene leading to the synthesis of a short polypeptide. The leaf transcriptome analysis showed that RcaS had a higher expression level than that of RcaL in a normal growth environment. In addition, the yeast two-hybrid assays showed the small isoform of Rubisco activase in close contact with the large subunit of the Rubisco in this species, supporting the side-on binding model of interaction between two proteins. This study broadens our understanding of the molecular characteristics of some essential genes in photosynthesis.</abstract><cop>Beijing</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1111/jse.12242</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1674-4918 |
ispartof | Journal of systematics and evolution : JSE, 2017-05, Vol.55 (3), p.200-207 |
issn | 1674-4918 1759-6831 |
language | eng |
recordid | cdi_proquest_journals_1897065898 |
source | Wiley Online Library All Journals |
subjects | Alternative splicing cDNA测序 Deoxyribonucleic acid DNA Economic analysis Economic models Economic planning Exons expression divergence Gene expression Genes Homology Introns Nucleotide sequence Oryza Photosynthesis protein interaction Proteins Ribulose-bisphosphate carboxylase Rubisco activase Rubisco活化酶 Splicing wild rice Yeast 光合作用 基因组DNA 经济植物 酶基因 鉴定 |
title | Identification and characterization of Rubisco activase genes in Oryza punctata |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-17T04%3A47%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Identification%20and%20characterization%20of%20Rubisco%20activase%20genes%20in%20Oryza%20punctata&rft.jtitle=Journal%20of%20systematics%20and%20evolution%20:%20JSE&rft.au=Xu,%20Si&rft.date=2017-05&rft.volume=55&rft.issue=3&rft.spage=200&rft.epage=207&rft.pages=200-207&rft.issn=1674-4918&rft.eissn=1759-6831&rft_id=info:doi/10.1111/jse.12242&rft_dat=%3Cproquest_cross%3E1897065898%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1897065898&rft_id=info:pmid/&rft_cqvip_id=672274893&rfr_iscdi=true |