Complementary DNA cloning of poplar bark storage protein and control of its expression by photoperiod.
Identifieur interne : 004C22 ( Main/Exploration ); précédent : 004C21; suivant : 004C23Complementary DNA cloning of poplar bark storage protein and control of its expression by photoperiod.
Auteurs : G D Coleman [États-Unis] ; T H Chen ; L H FuchigamiSource :
- Plant physiology [ 0032-0889 ] ; 1992.
Abstract
Bark storage proteins accumulate in the bark of many woody plants during autumn and winter. In poplar (Populus deltoides Bartr. ex Marsh), the accumulation of the 32-kilodalton bark storage protein is controlled by photoperiod. We have isolated a full-length cDNA encoding for the poplar 32-kilodalton bark storage protein and determined its nucleotide sequence. The derived amino acid sequence shows that poplar bark storage protein is rich in serine, leucine, phenylalanine, and lysine. Poplar bark storage protein is similar to the poplar wound-induced cDNA clone 4 and clone 16 (TJ Parsons, HD Bradshaw, MP Gordon [1989] Proc Natl Acad Sci USA 86: 7895-7899). DNA gel blot analysis suggests that poplar bark storage protein is encoded by a multigene family of about five genes. Poplar plants grown in long days contained low levels of mRNA for the bark storage protein. Exposure to short days resulted in an increase in bark storage protein mRNA within 7 days. After 21 days of short day exposure, high levels of mRNA were detected. The accumulation of bark storage protein mRNA in response to short days was also observed in plants exposed to natural shortening daylengths. Our results indicate that the accumulation of poplar bark storage protein mRNA is controlled by photoperiod. This finding will provide a useful system for investigating photoperiodism in woody plants.
DOI: 10.1104/pp.98.2.687
PubMed: 16668696
PubMed Central: PMC1080245
Affiliations:
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In poplar (Populus deltoides Bartr. ex Marsh), the accumulation of the 32-kilodalton bark storage protein is controlled by photoperiod. We have isolated a full-length cDNA encoding for the poplar 32-kilodalton bark storage protein and determined its nucleotide sequence. The derived amino acid sequence shows that poplar bark storage protein is rich in serine, leucine, phenylalanine, and lysine. Poplar bark storage protein is similar to the poplar wound-induced cDNA clone 4 and clone 16 (TJ Parsons, HD Bradshaw, MP Gordon [1989] Proc Natl Acad Sci USA 86: 7895-7899). DNA gel blot analysis suggests that poplar bark storage protein is encoded by a multigene family of about five genes. Poplar plants grown in long days contained low levels of mRNA for the bark storage protein. Exposure to short days resulted in an increase in bark storage protein mRNA within 7 days. After 21 days of short day exposure, high levels of mRNA were detected. The accumulation of bark storage protein mRNA in response to short days was also observed in plants exposed to natural shortening daylengths. Our results indicate that the accumulation of poplar bark storage protein mRNA is controlled by photoperiod. This finding will provide a useful system for investigating photoperiodism in woody plants.</div></front></TEI><pubmed><MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM"><PMID Version="1">16668696</PMID><DateCompleted><Year>2010</Year><Month>06</Month><Day>29</Day></DateCompleted><DateRevised><Year>2019</Year><Month>05</Month><Day>14</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Print">0032-0889</ISSN><JournalIssue CitedMedium="Print"><Volume>98</Volume><Issue>2</Issue><PubDate><Year>1992</Year><Month>Feb</Month></PubDate></JournalIssue><Title>Plant physiology</Title><ISOAbbreviation>Plant Physiol</ISOAbbreviation></Journal><ArticleTitle>Complementary DNA cloning of poplar bark storage protein and control of its expression by photoperiod.</ArticleTitle><Pagination><MedlinePgn>687-93</MedlinePgn></Pagination><Abstract><AbstractText>Bark storage proteins accumulate in the bark of many woody plants during autumn and winter. In poplar (Populus deltoides Bartr. ex Marsh), the accumulation of the 32-kilodalton bark storage protein is controlled by photoperiod. We have isolated a full-length cDNA encoding for the poplar 32-kilodalton bark storage protein and determined its nucleotide sequence. The derived amino acid sequence shows that poplar bark storage protein is rich in serine, leucine, phenylalanine, and lysine. Poplar bark storage protein is similar to the poplar wound-induced cDNA clone 4 and clone 16 (TJ Parsons, HD Bradshaw, MP Gordon [1989] Proc Natl Acad Sci USA 86: 7895-7899). DNA gel blot analysis suggests that poplar bark storage protein is encoded by a multigene family of about five genes. Poplar plants grown in long days contained low levels of mRNA for the bark storage protein. Exposure to short days resulted in an increase in bark storage protein mRNA within 7 days. After 21 days of short day exposure, high levels of mRNA were detected. The accumulation of bark storage protein mRNA in response to short days was also observed in plants exposed to natural shortening daylengths. Our results indicate that the accumulation of poplar bark storage protein mRNA is controlled by photoperiod. This finding will provide a useful system for investigating photoperiodism in woody plants.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Coleman</LastName><ForeName>G D</ForeName><Initials>GD</Initials><AffiliationInfo><Affiliation>Department of Horticulture, Oregon State University, Corvallis, Oregon 97331.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Chen</LastName><ForeName>T H</ForeName><Initials>TH</Initials></Author><Author ValidYN="Y"><LastName>Fuchigami</LastName><ForeName>L H</ForeName><Initials>LH</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Plant Physiol</MedlineTA><NlmUniqueID>0401224</NlmUniqueID><ISSNLinking>0032-0889</ISSNLinking></MedlineJournalInfo></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1992</Year><Month>2</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>1992</Year><Month>2</Month><Day>1</Day><Hour>0</Hour><Minute>1</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>1992</Year><Month>2</Month><Day>1</Day><Hour>0</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">16668696</ArticleId><ArticleId IdType="pmc">PMC1080245</ArticleId><ArticleId IdType="doi">10.1104/pp.98.2.687</ArticleId></ArticleIdList><ReferenceList><Reference><Citation>Science. 1970 Sep 25;169(3952):1269-78</Citation><ArticleIdList><ArticleId IdType="pubmed">17772511</ArticleId></ArticleIdList></Reference><Reference><Citation>Proc Natl Acad Sci U S A. 1988 Apr;85(8):2444-8</Citation><ArticleIdList><ArticleId IdType="pubmed">3162770</ArticleId></ArticleIdList></Reference><Reference><Citation>Proc Natl Acad Sci U S A. 1989 Oct;86(20):7895-9</Citation><ArticleIdList><ArticleId IdType="pubmed">2813366</ArticleId></ArticleIdList></Reference><Reference><Citation>Plant Physiol. 1989 Aug;90(4):1252-5</Citation><ArticleIdList><ArticleId IdType="pubmed">16666917</ArticleId></ArticleIdList></Reference><Reference><Citation>Plant Physiol. 1989 Jan;89(1):309-15</Citation><ArticleIdList><ArticleId IdType="pubmed">16666532</ArticleId></ArticleIdList></Reference><Reference><Citation>Plant Physiol. 1983 Jan;71(1):161-8</Citation><ArticleIdList><ArticleId IdType="pubmed">16662778</ArticleId></ArticleIdList></Reference><Reference><Citation>Plant Mol Biol. 1989 Oct;13(4):347-54</Citation><ArticleIdList><ArticleId IdType="pubmed">2491661</ArticleId></ArticleIdList></Reference><Reference><Citation>Plant Physiol. 1974 Oct;54(4):544-9</Citation><ArticleIdList><ArticleId IdType="pubmed">16658925</ArticleId></ArticleIdList></Reference><Reference><Citation>J Mol Biol. 1975 Nov 5;98(3):503-17</Citation><ArticleIdList><ArticleId IdType="pubmed">1195397</ArticleId></ArticleIdList></Reference><Reference><Citation>Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463-7</Citation><ArticleIdList><ArticleId IdType="pubmed">271968</ArticleId></ArticleIdList></Reference><Reference><Citation>Plant Physiol. 1991 Jul;96(3):686-92</Citation><ArticleIdList><ArticleId IdType="pubmed">16668243</ArticleId></ArticleIdList></Reference><Reference><Citation>Plant Physiol. 1986 Mar;80(3):747-51</Citation><ArticleIdList><ArticleId IdType="pubmed">16664696</ArticleId></ArticleIdList></Reference><Reference><Citation>Nucleic Acids Res. 1987 Aug 25;15(16):6643-53</Citation><ArticleIdList><ArticleId IdType="pubmed">3628002</ArticleId></ArticleIdList></Reference><Reference><Citation>Plant Cell. 1990 Jan;2(1):1-6</Citation><ArticleIdList><ArticleId IdType="pubmed">12354941</ArticleId></ArticleIdList></Reference><Reference><Citation>Nucleic Acids Res. 1988 Aug 11;16(15):7583-600</Citation><ArticleIdList><ArticleId IdType="pubmed">2970625</ArticleId></ArticleIdList></Reference><Reference><Citation>Methods Enzymol. 1987;155:156-65</Citation><ArticleIdList><ArticleId IdType="pubmed">3323819</ArticleId></ArticleIdList></Reference></ReferenceList></PubmedData></pubmed><affiliations><list><country><li>États-Unis</li></country><region><li>Oregon</li></region></list><tree><noCountry><name sortKey="Chen, T H" sort="Chen, T H" uniqKey="Chen T" first="T H" last="Chen">T H Chen</name><name sortKey="Fuchigami, L H" sort="Fuchigami, L H" uniqKey="Fuchigami L" first="L H" last="Fuchigami">L H Fuchigami</name></noCountry><country name="États-Unis"><region name="Oregon"><name sortKey="Coleman, G D" sort="Coleman, G D" uniqKey="Coleman G" first="G D" last="Coleman">G D Coleman</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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