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Is the LIM-domain Protein HaWLIM1 Associated with Cortical Microtubules in Sunflower Protoplasts?
Flowering plants express several LIM-domain proteins related to the animal cystein-rich proteins. The expression of sunflower LIM genes was followed by RT-PCR in cultured sunflower protoplasts. A transcript was detected only for HaWLIM1, but not for the other two genes HaPLIM1 and HaPLIM2. Polyclona...
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Published in: | Plant and cell physiology 2003-10, Vol.44 (10), p.1055-1063 |
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description | Flowering plants express several LIM-domain proteins related to the animal cystein-rich proteins. The expression of sunflower LIM genes was followed by RT-PCR in cultured sunflower protoplasts. A transcript was detected only for HaWLIM1, but not for the other two genes HaPLIM1 and HaPLIM2. Polyclonal antibodies raised against either full length recombinant HaWLIM1 protein or peptides recognized a 27 kDa polypeptide on Western blots. Immunocytolocalization studies showed that HaWLIM1 is located in the cytoplasm and in the nucleus. In the cytoplasm, HaWLIM1 is localized in punctate structures, distributed along microtubule bundles. Depolymerizing microtubules with oryzalin resulted in a strong modification of the HaWLIM1 cortical pattern. In contrast, treatment of protoplasts with latrunculin B, which disrupts actin filaments, had no effect on HaWLIM1 localization. HaWLIM1 was also located within the nucleus of interphase protoplasts. During mitosis, nuclear labelling was observed in prophase, which decreased in metaphase, disappeared in anaphase, and recovered in telophase. These results suggest a dual role for HaWLIM1: in the cytoplasm, as a component of molecular complexes which may interact with microtubules, and in the nucleus, as a partner of transcription factors during interphase. |
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The expression of sunflower LIM genes was followed by RT-PCR in cultured sunflower protoplasts. A transcript was detected only for HaWLIM1, but not for the other two genes HaPLIM1 and HaPLIM2. Polyclonal antibodies raised against either full length recombinant HaWLIM1 protein or peptides recognized a 27 kDa polypeptide on Western blots. Immunocytolocalization studies showed that HaWLIM1 is located in the cytoplasm and in the nucleus. In the cytoplasm, HaWLIM1 is localized in punctate structures, distributed along microtubule bundles. Depolymerizing microtubules with oryzalin resulted in a strong modification of the HaWLIM1 cortical pattern. In contrast, treatment of protoplasts with latrunculin B, which disrupts actin filaments, had no effect on HaWLIM1 localization. HaWLIM1 was also located within the nucleus of interphase protoplasts. During mitosis, nuclear labelling was observed in prophase, which decreased in metaphase, disappeared in anaphase, and recovered in telophase. These results suggest a dual role for HaWLIM1: in the cytoplasm, as a component of molecular complexes which may interact with microtubules, and in the nucleus, as a partner of transcription factors during interphase.</description><identifier>ISSN: 0032-0781</identifier><identifier>EISSN: 1471-9053</identifier><identifier>DOI: 10.1093/pcp/pcg126</identifier><identifier>PMID: 14581630</identifier><language>eng</language><publisher>Japan: Oxford University Press</publisher><subject>Base Sequence ; Cellular Biology ; CRP ; cystein-rich protein ; DNA Primers ; Gene Expression Regulation, Plant ; Helianthus - genetics ; Helianthus - physiology ; Homeodomain Proteins - analysis ; Homeodomain Proteins - genetics ; Image Processing, Computer-Assisted ; Keywords: Helianthus annuus — LIM-domain protein — Microtubule — Protoplast — Sunflower ; Life Sciences ; Microscopy, Fluorescence ; Microtubules - ultrastructure ; Plant Growth Regulators - analysis ; Plant Growth Regulators - genetics ; Plant Proteins - analysis ; Plant Proteins - genetics ; Protoplasts - ultrastructure ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Plant - genetics ; RNA, Plant - isolation & purification ; Zinc Fingers</subject><ispartof>Plant and cell physiology, 2003-10, Vol.44 (10), p.1055-1063</ispartof><rights>Copyright Oxford University Press(England) Oct 15, 2003</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-8dac436b47a2d8433217556e57578ee218c7eef26afb65d937e0cf7e9cc20e43</citedby><cites>FETCH-LOGICAL-c418t-8dac436b47a2d8433217556e57578ee218c7eef26afb65d937e0cf7e9cc20e43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14581630$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00023080$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Brière, Christian</creatorcontrib><creatorcontrib>Bordel, Anne-Claire</creatorcontrib><creatorcontrib>Barthou, Henri</creatorcontrib><creatorcontrib>Jauneau, Alain</creatorcontrib><creatorcontrib>Steinmetz, André</creatorcontrib><creatorcontrib>Alibert, Gilbert</creatorcontrib><creatorcontrib>Petitprez, Michel</creatorcontrib><title>Is the LIM-domain Protein HaWLIM1 Associated with Cortical Microtubules in Sunflower Protoplasts?</title><title>Plant and cell physiology</title><addtitle>Plant Cell Physiol</addtitle><description>Flowering plants express several LIM-domain proteins related to the animal cystein-rich proteins. The expression of sunflower LIM genes was followed by RT-PCR in cultured sunflower protoplasts. A transcript was detected only for HaWLIM1, but not for the other two genes HaPLIM1 and HaPLIM2. Polyclonal antibodies raised against either full length recombinant HaWLIM1 protein or peptides recognized a 27 kDa polypeptide on Western blots. Immunocytolocalization studies showed that HaWLIM1 is located in the cytoplasm and in the nucleus. In the cytoplasm, HaWLIM1 is localized in punctate structures, distributed along microtubule bundles. Depolymerizing microtubules with oryzalin resulted in a strong modification of the HaWLIM1 cortical pattern. In contrast, treatment of protoplasts with latrunculin B, which disrupts actin filaments, had no effect on HaWLIM1 localization. HaWLIM1 was also located within the nucleus of interphase protoplasts. During mitosis, nuclear labelling was observed in prophase, which decreased in metaphase, disappeared in anaphase, and recovered in telophase. These results suggest a dual role for HaWLIM1: in the cytoplasm, as a component of molecular complexes which may interact with microtubules, and in the nucleus, as a partner of transcription factors during interphase.</description><subject>Base Sequence</subject><subject>Cellular Biology</subject><subject>CRP</subject><subject>cystein-rich protein</subject><subject>DNA Primers</subject><subject>Gene Expression Regulation, Plant</subject><subject>Helianthus - genetics</subject><subject>Helianthus - physiology</subject><subject>Homeodomain Proteins - analysis</subject><subject>Homeodomain Proteins - genetics</subject><subject>Image Processing, Computer-Assisted</subject><subject>Keywords: Helianthus annuus — LIM-domain protein — Microtubule — Protoplast — Sunflower</subject><subject>Life Sciences</subject><subject>Microscopy, Fluorescence</subject><subject>Microtubules - ultrastructure</subject><subject>Plant Growth Regulators - analysis</subject><subject>Plant Growth Regulators - genetics</subject><subject>Plant Proteins - analysis</subject><subject>Plant Proteins - genetics</subject><subject>Protoplasts - ultrastructure</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Plant - genetics</subject><subject>RNA, Plant - isolation & purification</subject><subject>Zinc Fingers</subject><issn>0032-0781</issn><issn>1471-9053</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNpdkV9rFDEUxYNY7Fp98QPI4ENBYfTm_-yTLFvrLkyxYEHxJWQzd9zU2c04yVj99madpQUfLvdy8ssJN4eQFxTeUpjzd73rc32nTD0iMyo0Lecg-WMyA-CsBF3RU_I0xluAPHN4Qk6pkBVVHGbErmORtljU66uyCTvr98X1EBLmvrJfskqLRYzBeZuwKe582hbLMCTvbFdceZfRcTN2GIt84fO4b7twh8M_i9B3Nqb4_hk5aW0X8fmxn5Gbyw83y1VZf_q4Xi7q0glapbJqrBNcbYS2rKkE54xqKRVKLXWFyGjlNGLLlG03SjZzrhFcq3HuHAMU_Iy8nmy3tjP94Hd2-GOC9Wa1qM1By9szDhX8opk9n9h-CD9HjMnsfHTYdXaPYYxGUw5aqAP46j_wNozDPq9hGFCpBJUyQ28mKP9GjAO2989TMIeATA7ITAFl-OXRcdzssHlAj4lkoJwAHxP-vj-3ww-jNNfSrL5-M6AuL64Vqw3jfwFB-5m0</recordid><startdate>20031001</startdate><enddate>20031001</enddate><creator>Brière, Christian</creator><creator>Bordel, Anne-Claire</creator><creator>Barthou, Henri</creator><creator>Jauneau, Alain</creator><creator>Steinmetz, André</creator><creator>Alibert, Gilbert</creator><creator>Petitprez, Michel</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><general>Oxford University Press (OUP)</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7QP</scope><scope>7T5</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope></search><sort><creationdate>20031001</creationdate><title>Is the LIM-domain Protein HaWLIM1 Associated with Cortical Microtubules in Sunflower Protoplasts?</title><author>Brière, Christian ; Bordel, Anne-Claire ; Barthou, Henri ; Jauneau, Alain ; Steinmetz, André ; Alibert, Gilbert ; Petitprez, Michel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-8dac436b47a2d8433217556e57578ee218c7eef26afb65d937e0cf7e9cc20e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Base Sequence</topic><topic>Cellular Biology</topic><topic>CRP</topic><topic>cystein-rich protein</topic><topic>DNA Primers</topic><topic>Gene Expression Regulation, Plant</topic><topic>Helianthus - genetics</topic><topic>Helianthus - physiology</topic><topic>Homeodomain Proteins - analysis</topic><topic>Homeodomain Proteins - genetics</topic><topic>Image Processing, Computer-Assisted</topic><topic>Keywords: Helianthus annuus — LIM-domain protein — Microtubule — Protoplast — Sunflower</topic><topic>Life Sciences</topic><topic>Microscopy, Fluorescence</topic><topic>Microtubules - ultrastructure</topic><topic>Plant Growth Regulators - analysis</topic><topic>Plant Growth Regulators - genetics</topic><topic>Plant Proteins - analysis</topic><topic>Plant Proteins - genetics</topic><topic>Protoplasts - ultrastructure</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Plant - genetics</topic><topic>RNA, Plant - isolation & purification</topic><topic>Zinc Fingers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brière, Christian</creatorcontrib><creatorcontrib>Bordel, Anne-Claire</creatorcontrib><creatorcontrib>Barthou, Henri</creatorcontrib><creatorcontrib>Jauneau, Alain</creatorcontrib><creatorcontrib>Steinmetz, André</creatorcontrib><creatorcontrib>Alibert, Gilbert</creatorcontrib><creatorcontrib>Petitprez, Michel</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Plant and cell physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brière, Christian</au><au>Bordel, Anne-Claire</au><au>Barthou, Henri</au><au>Jauneau, Alain</au><au>Steinmetz, André</au><au>Alibert, Gilbert</au><au>Petitprez, Michel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Is the LIM-domain Protein HaWLIM1 Associated with Cortical Microtubules in Sunflower Protoplasts?</atitle><jtitle>Plant and cell physiology</jtitle><addtitle>Plant Cell Physiol</addtitle><date>2003-10-01</date><risdate>2003</risdate><volume>44</volume><issue>10</issue><spage>1055</spage><epage>1063</epage><pages>1055-1063</pages><issn>0032-0781</issn><eissn>1471-9053</eissn><abstract>Flowering plants express several LIM-domain proteins related to the animal cystein-rich proteins. The expression of sunflower LIM genes was followed by RT-PCR in cultured sunflower protoplasts. A transcript was detected only for HaWLIM1, but not for the other two genes HaPLIM1 and HaPLIM2. Polyclonal antibodies raised against either full length recombinant HaWLIM1 protein or peptides recognized a 27 kDa polypeptide on Western blots. Immunocytolocalization studies showed that HaWLIM1 is located in the cytoplasm and in the nucleus. In the cytoplasm, HaWLIM1 is localized in punctate structures, distributed along microtubule bundles. Depolymerizing microtubules with oryzalin resulted in a strong modification of the HaWLIM1 cortical pattern. In contrast, treatment of protoplasts with latrunculin B, which disrupts actin filaments, had no effect on HaWLIM1 localization. HaWLIM1 was also located within the nucleus of interphase protoplasts. During mitosis, nuclear labelling was observed in prophase, which decreased in metaphase, disappeared in anaphase, and recovered in telophase. These results suggest a dual role for HaWLIM1: in the cytoplasm, as a component of molecular complexes which may interact with microtubules, and in the nucleus, as a partner of transcription factors during interphase.</abstract><cop>Japan</cop><pub>Oxford University Press</pub><pmid>14581630</pmid><doi>10.1093/pcp/pcg126</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Base Sequence Cellular Biology CRP cystein-rich protein DNA Primers Gene Expression Regulation, Plant Helianthus - genetics Helianthus - physiology Homeodomain Proteins - analysis Homeodomain Proteins - genetics Image Processing, Computer-Assisted Keywords: Helianthus annuus — LIM-domain protein — Microtubule — Protoplast — Sunflower Life Sciences Microscopy, Fluorescence Microtubules - ultrastructure Plant Growth Regulators - analysis Plant Growth Regulators - genetics Plant Proteins - analysis Plant Proteins - genetics Protoplasts - ultrastructure Reverse Transcriptase Polymerase Chain Reaction RNA, Plant - genetics RNA, Plant - isolation & purification Zinc Fingers |
title | Is the LIM-domain Protein HaWLIM1 Associated with Cortical Microtubules in Sunflower Protoplasts? |
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