novel family of plant splicing factors with a Zn knuckle motif: examination of RNA binding and splicing activities
An important group of splicing factors involved in constitutive and alternative splicing contain an arginine/serine (RS)-rich domain. We have previously demonstrated the existence of such factors in plants and report now on a new family of splicing factors (termed the RSZ family) from Arabidopsis th...
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Veröffentlicht in: | Plant molecular biology 1999-03, Vol.39 (4), p.761-773 |
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description | An important group of splicing factors involved in constitutive and alternative splicing contain an arginine/serine (RS)-rich domain. We have previously demonstrated the existence of such factors in plants and report now on a new family of splicing factors (termed the RSZ family) from Arabidopsis thaliana which additionally harbor a Zn knuckle motif similar to the human splicing factor 9G8. Although only around 20 kDa in size, members of this family possess a multi-domain structure. In addition to the N-terminal RNA recognition motif (RRM), a Zn finger motif of the CCHC-type is inserted in an RGG-rich region; all three motifs are known to contribute to RNA binding. The C-terminal domain has a characteristic repeated structure which is very arginine-rich and centered around an SP dipeptide. One member of this family, atRSZp22, has been shown to be a phosphoprotein with properties similar to SR proteins. Furthermore, atRSZp22 was able to complement efficiently splicing deficient mammalian S100 as well as h9G8-depleted extracts. RNA binding assays to selected RNA sequences indicate an RNA binding specificity similar to the human splicing factors 9G8 and SRp20. Taken together, these result show that atRSZp22 is a true plant splicing factor which combines structural and functional features of both h9g8 and hSRp20. |
doi_str_mv | 10.1023/A:1006129615846 |
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We have previously demonstrated the existence of such factors in plants and report now on a new family of splicing factors (termed the RSZ family) from Arabidopsis thaliana which additionally harbor a Zn knuckle motif similar to the human splicing factor 9G8. Although only around 20 kDa in size, members of this family possess a multi-domain structure. In addition to the N-terminal RNA recognition motif (RRM), a Zn finger motif of the CCHC-type is inserted in an RGG-rich region; all three motifs are known to contribute to RNA binding. The C-terminal domain has a characteristic repeated structure which is very arginine-rich and centered around an SP dipeptide. One member of this family, atRSZp22, has been shown to be a phosphoprotein with properties similar to SR proteins. Furthermore, atRSZp22 was able to complement efficiently splicing deficient mammalian S100 as well as h9G8-depleted extracts. RNA binding assays to selected RNA sequences indicate an RNA binding specificity similar to the human splicing factors 9G8 and SRp20. Taken together, these result show that atRSZp22 is a true plant splicing factor which combines structural and functional features of both h9g8 and hSRp20.</description><identifier>ISSN: 0167-4412</identifier><identifier>EISSN: 1573-5028</identifier><identifier>DOI: 10.1023/A:1006129615846</identifier><identifier>PMID: 10350090</identifier><language>eng</language><publisher>Netherlands: Springer Nature B.V</publisher><subject>Alternative Splicing ; Amino Acid Sequence ; amino acid sequences ; Animals ; Arabidopsis - genetics ; Arabidopsis - metabolism ; Arabidopsis Proteins ; Arabidopsis thaliana ; Base Sequence ; binding ; binding proteins ; Binding Sites ; Cloning, Molecular ; Genes, Plant ; Genomics ; Humans ; Life Sciences ; Mammals ; messenger RNA ; Molecular Sequence Data ; Multigene Family ; Peptides ; Plant biology ; precursors ; Recombinant Proteins - chemistry ; Recombinant Proteins - metabolism ; Ribonucleic acid ; RNA ; rna recognition motifs ; RNA Splicing ; RNA-Binding Proteins - chemistry ; RNA-Binding Proteins - genetics ; RNA-Binding Proteins - metabolism ; Sequence Alignment ; Sequence Homology, Amino Acid ; Serine-Arginine Splicing Factors ; Vegetal Biology ; Zinc ; Zinc Fingers</subject><ispartof>Plant molecular biology, 1999-03, Vol.39 (4), p.761-773</ispartof><rights>Kluwer Academic Publishers 1999</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c369t-c365d8ddf541448bb24a8157b9eeb2d24e188f1a09bfeeb497372d0b80569a103</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10350090$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03991566$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Lopato, S</creatorcontrib><creatorcontrib>Gattoni, R</creatorcontrib><creatorcontrib>Fabini, G</creatorcontrib><creatorcontrib>Stevenin, J</creatorcontrib><creatorcontrib>Barta, A</creatorcontrib><title>novel family of plant splicing factors with a Zn knuckle motif: examination of RNA binding and splicing activities</title><title>Plant molecular biology</title><addtitle>Plant Mol Biol</addtitle><description>An important group of splicing factors involved in constitutive and alternative splicing contain an arginine/serine (RS)-rich domain. We have previously demonstrated the existence of such factors in plants and report now on a new family of splicing factors (termed the RSZ family) from Arabidopsis thaliana which additionally harbor a Zn knuckle motif similar to the human splicing factor 9G8. Although only around 20 kDa in size, members of this family possess a multi-domain structure. In addition to the N-terminal RNA recognition motif (RRM), a Zn finger motif of the CCHC-type is inserted in an RGG-rich region; all three motifs are known to contribute to RNA binding. The C-terminal domain has a characteristic repeated structure which is very arginine-rich and centered around an SP dipeptide. One member of this family, atRSZp22, has been shown to be a phosphoprotein with properties similar to SR proteins. Furthermore, atRSZp22 was able to complement efficiently splicing deficient mammalian S100 as well as h9G8-depleted extracts. RNA binding assays to selected RNA sequences indicate an RNA binding specificity similar to the human splicing factors 9G8 and SRp20. Taken together, these result show that atRSZp22 is a true plant splicing factor which combines structural and functional features of both h9g8 and hSRp20.</description><subject>Alternative Splicing</subject><subject>Amino Acid Sequence</subject><subject>amino acid sequences</subject><subject>Animals</subject><subject>Arabidopsis - genetics</subject><subject>Arabidopsis - metabolism</subject><subject>Arabidopsis Proteins</subject><subject>Arabidopsis thaliana</subject><subject>Base Sequence</subject><subject>binding</subject><subject>binding proteins</subject><subject>Binding Sites</subject><subject>Cloning, Molecular</subject><subject>Genes, Plant</subject><subject>Genomics</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Mammals</subject><subject>messenger RNA</subject><subject>Molecular Sequence Data</subject><subject>Multigene Family</subject><subject>Peptides</subject><subject>Plant biology</subject><subject>precursors</subject><subject>Recombinant Proteins - chemistry</subject><subject>Recombinant Proteins - metabolism</subject><subject>Ribonucleic acid</subject><subject>RNA</subject><subject>rna recognition motifs</subject><subject>RNA Splicing</subject><subject>RNA-Binding Proteins - chemistry</subject><subject>RNA-Binding Proteins - genetics</subject><subject>RNA-Binding Proteins - metabolism</subject><subject>Sequence Alignment</subject><subject>Sequence Homology, Amino Acid</subject><subject>Serine-Arginine Splicing Factors</subject><subject>Vegetal Biology</subject><subject>Zinc</subject><subject>Zinc Fingers</subject><issn>0167-4412</issn><issn>1573-5028</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkc1v1DAQxS0EotvCmRtYHJA4LMz4M-5tVQFFWoEE9MLFchKndZvYS5ws7X-Poy0gceEyI41_72nemJBnCG8QGH-7OUUAhcwolJVQD8gKpeZrCax6SFaASq-FQHZEjnO-BigwV4_JEQKXAAZWZIxp73vauSH0dzR1dNe7ONG860MT4mV5aKY0ZvozTFfU0e-R3sS5uek9HdIUulPqb4s0uimkuMi_fNrQOsR20brY_jUqPmEfpuDzE_Koc332T-_7Cbl4_-7b2fl6-_nDx7PNdt1wZaalyrZq204KFKKqayZcVdLVxvuatUx4rKoOHZi6KxNhNNeshboCqYwrCU_I64PvlevtbgyDG-9scsGeb7Z2mQE3BqVSeyzsqwO7G9OP2efJDiE3vi_H8GnOVhltEMpp_weiZhwRFseX_4DXaR5jCWy1RiEF47JAz--huR58-2fL3_9TgBcHoHPJussxZHvxlRV7YAaFUpr_AsA1mZ8</recordid><startdate>19990301</startdate><enddate>19990301</enddate><creator>Lopato, S</creator><creator>Gattoni, R</creator><creator>Fabini, G</creator><creator>Stevenin, J</creator><creator>Barta, A</creator><general>Springer Nature B.V</general><general>Springer Verlag (Germany)</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope></search><sort><creationdate>19990301</creationdate><title>novel family of plant splicing factors with a Zn knuckle motif: examination of RNA binding and splicing activities</title><author>Lopato, S ; Gattoni, R ; Fabini, G ; Stevenin, J ; Barta, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c369t-c365d8ddf541448bb24a8157b9eeb2d24e188f1a09bfeeb497372d0b80569a103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Alternative Splicing</topic><topic>Amino Acid Sequence</topic><topic>amino acid sequences</topic><topic>Animals</topic><topic>Arabidopsis - genetics</topic><topic>Arabidopsis - metabolism</topic><topic>Arabidopsis Proteins</topic><topic>Arabidopsis thaliana</topic><topic>Base Sequence</topic><topic>binding</topic><topic>binding proteins</topic><topic>Binding Sites</topic><topic>Cloning, Molecular</topic><topic>Genes, Plant</topic><topic>Genomics</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Mammals</topic><topic>messenger RNA</topic><topic>Molecular Sequence Data</topic><topic>Multigene Family</topic><topic>Peptides</topic><topic>Plant biology</topic><topic>precursors</topic><topic>Recombinant Proteins - chemistry</topic><topic>Recombinant Proteins - metabolism</topic><topic>Ribonucleic acid</topic><topic>RNA</topic><topic>rna recognition motifs</topic><topic>RNA Splicing</topic><topic>RNA-Binding Proteins - chemistry</topic><topic>RNA-Binding Proteins - genetics</topic><topic>RNA-Binding Proteins - metabolism</topic><topic>Sequence Alignment</topic><topic>Sequence Homology, Amino Acid</topic><topic>Serine-Arginine Splicing Factors</topic><topic>Vegetal Biology</topic><topic>Zinc</topic><topic>Zinc Fingers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lopato, S</creatorcontrib><creatorcontrib>Gattoni, R</creatorcontrib><creatorcontrib>Fabini, G</creatorcontrib><creatorcontrib>Stevenin, J</creatorcontrib><creatorcontrib>Barta, A</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</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>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</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 Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Plant molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lopato, S</au><au>Gattoni, R</au><au>Fabini, G</au><au>Stevenin, J</au><au>Barta, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>novel family of plant splicing factors with a Zn knuckle motif: examination of RNA binding and splicing activities</atitle><jtitle>Plant molecular biology</jtitle><addtitle>Plant Mol Biol</addtitle><date>1999-03-01</date><risdate>1999</risdate><volume>39</volume><issue>4</issue><spage>761</spage><epage>773</epage><pages>761-773</pages><issn>0167-4412</issn><eissn>1573-5028</eissn><abstract>An important group of splicing factors involved in constitutive and alternative splicing contain an arginine/serine (RS)-rich domain. We have previously demonstrated the existence of such factors in plants and report now on a new family of splicing factors (termed the RSZ family) from Arabidopsis thaliana which additionally harbor a Zn knuckle motif similar to the human splicing factor 9G8. Although only around 20 kDa in size, members of this family possess a multi-domain structure. In addition to the N-terminal RNA recognition motif (RRM), a Zn finger motif of the CCHC-type is inserted in an RGG-rich region; all three motifs are known to contribute to RNA binding. The C-terminal domain has a characteristic repeated structure which is very arginine-rich and centered around an SP dipeptide. One member of this family, atRSZp22, has been shown to be a phosphoprotein with properties similar to SR proteins. Furthermore, atRSZp22 was able to complement efficiently splicing deficient mammalian S100 as well as h9G8-depleted extracts. RNA binding assays to selected RNA sequences indicate an RNA binding specificity similar to the human splicing factors 9G8 and SRp20. Taken together, these result show that atRSZp22 is a true plant splicing factor which combines structural and functional features of both h9g8 and hSRp20.</abstract><cop>Netherlands</cop><pub>Springer Nature B.V</pub><pmid>10350090</pmid><doi>10.1023/A:1006129615846</doi><tpages>13</tpages></addata></record> |
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subjects | Alternative Splicing Amino Acid Sequence amino acid sequences Animals Arabidopsis - genetics Arabidopsis - metabolism Arabidopsis Proteins Arabidopsis thaliana Base Sequence binding binding proteins Binding Sites Cloning, Molecular Genes, Plant Genomics Humans Life Sciences Mammals messenger RNA Molecular Sequence Data Multigene Family Peptides Plant biology precursors Recombinant Proteins - chemistry Recombinant Proteins - metabolism Ribonucleic acid RNA rna recognition motifs RNA Splicing RNA-Binding Proteins - chemistry RNA-Binding Proteins - genetics RNA-Binding Proteins - metabolism Sequence Alignment Sequence Homology, Amino Acid Serine-Arginine Splicing Factors Vegetal Biology Zinc Zinc Fingers |
title | novel family of plant splicing factors with a Zn knuckle motif: examination of RNA binding and splicing activities |
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