Persian sturgeon insulin-like growth factor I: molecular cloning and expression during various nutritional conditions.
Identifieur interne : 000191 ( PubMed/Curation ); précédent : 000190; suivant : 000192Persian sturgeon insulin-like growth factor I: molecular cloning and expression during various nutritional conditions.
Auteurs : Mahtab Yarmohammadi [Oman] ; Mohammad Pourkazemi ; Rezvanollah Kazemi ; Ali Hallajian ; Hassan Soltanloo ; Mohammad Hassanzadeh Saber ; Alireza AbbasalizadehSource :
- Journal of applied genetics [ 2190-3883 ] ; 2014.
English descriptors
- KwdEn :
- Amino Acid Sequence, Animal Nutritional Physiological Phenomena (genetics), Animals, Body Weight (genetics), Cloning, Molecular, DNA, Complementary (genetics), Fishes (genetics), Fishes (growth & development), Gene Expression Regulation, Insulin-Like Growth Factor I (chemistry), Insulin-Like Growth Factor I (genetics), Insulin-Like Growth Factor I (metabolism), Molecular Sequence Data, Persia, Phylogeny, RNA, Messenger (genetics), RNA, Messenger (metabolism), Sequence Analysis, DNA.
- MESH :
- chemical , chemistry : Insulin-Like Growth Factor I.
- chemical , genetics : DNA, Complementary, Insulin-Like Growth Factor I, RNA, Messenger.
- chemical , metabolism : RNA, Messenger.
- geographic : Persia.
- genetics : Animal Nutritional Physiological Phenomena, Body Weight, Fishes.
- growth & development : Fishes.
- chemical , metabolism : Insulin-Like Growth Factor I.
- Amino Acid Sequence, Animals, Cloning, Molecular, Gene Expression Regulation, Molecular Sequence Data, Phylogeny, Sequence Analysis, DNA.
Abstract
The effects of different periods of starvation (1, 2, 3, and 4 weeks) and subsequent re-feeding (over a 4 week) on the compensatory growth performance and insulin-like growth factor I (IGF-I) mRNA expression in liver and white muscle were investigated in juvenile Persian sturgeon (Acipenser persicus). First, a fragment of 617 nucleotides coding for IGF-I was cloned from liver, which included an open reading frame of 486 nucleotides, encoding a 162 amino acid preproIGF-I. This is composed of a 45 aa for signal peptide, a 117 aa for the mature peptide comprising the B, C, A, and D domains, and a 47 aa for E domain. The mature Persian sturgeon IGF-I exhibits high sequence identities with other sturgeon species and teleost, ranging between 68 and 95 %. The pattern of IGF-I mRNA expression in the liver and white muscle was measured in response to different periods of starvation and subsequent re-feeding. Nutritional status influenced IGF-I mRNA expression pattern in both liver and muscle. IGF-I mRNA expression in the liver increased during starvation, before decreasing after re-feeding. Furthermore, white muscle IGF-I mRNA expression showed better responses to nutritional status and decreased following starvation and increased by re-feeding. However, changes in the expression of IGF-I mRNA were not significantly different between any of the treatments in both tissues. These data suggest that muscle and liver IGF-I mRNA expression do not have a regulatory role for somatic growth induced by compensatory growth in Persain sturgeon.
DOI: 10.1007/s13353-013-0192-7
PubMed: 24430509
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Kazemi</name></author><author><name sortKey="Hallajian, Ali" sort="Hallajian, Ali" uniqKey="Hallajian A" first="Ali" last="Hallajian">Ali Hallajian</name></author><author><name sortKey="Soltanloo, Hassan" sort="Soltanloo, Hassan" uniqKey="Soltanloo H" first="Hassan" last="Soltanloo">Hassan Soltanloo</name></author><author><name sortKey="Hassanzadeh Saber, Mohammad" sort="Hassanzadeh Saber, Mohammad" uniqKey="Hassanzadeh Saber M" first="Mohammad" last="Hassanzadeh Saber">Mohammad Hassanzadeh Saber</name></author><author><name sortKey="Abbasalizadeh, Alireza" sort="Abbasalizadeh, Alireza" uniqKey="Abbasalizadeh A" first="Alireza" last="Abbasalizadeh">Alireza Abbasalizadeh</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2014">2014</date><idno type="RBID">pubmed:24430509</idno><idno type="pmid">24430509</idno><idno type="doi">10.1007/s13353-013-0192-7</idno><idno type="wicri:Area/PubMed/Corpus">000191</idno><idno type="wicri:explorRef" 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uniqKey="Pourkazemi M" first="Mohammad" last="Pourkazemi">Mohammad Pourkazemi</name></author><author><name sortKey="Kazemi, Rezvanollah" sort="Kazemi, Rezvanollah" uniqKey="Kazemi R" first="Rezvanollah" last="Kazemi">Rezvanollah Kazemi</name></author><author><name sortKey="Hallajian, Ali" sort="Hallajian, Ali" uniqKey="Hallajian A" first="Ali" last="Hallajian">Ali Hallajian</name></author><author><name sortKey="Soltanloo, Hassan" sort="Soltanloo, Hassan" uniqKey="Soltanloo H" first="Hassan" last="Soltanloo">Hassan Soltanloo</name></author><author><name sortKey="Hassanzadeh Saber, Mohammad" sort="Hassanzadeh Saber, Mohammad" uniqKey="Hassanzadeh Saber M" first="Mohammad" last="Hassanzadeh Saber">Mohammad Hassanzadeh Saber</name></author><author><name sortKey="Abbasalizadeh, Alireza" sort="Abbasalizadeh, Alireza" uniqKey="Abbasalizadeh A" first="Alireza" last="Abbasalizadeh">Alireza Abbasalizadeh</name></author></analytic><series><title level="j">Journal of applied genetics</title><idno type="eISSN">2190-3883</idno><imprint><date when="2014" type="published">2014</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Amino Acid Sequence</term><term>Animal Nutritional Physiological Phenomena (genetics)</term><term>Animals</term><term>Body Weight (genetics)</term><term>Cloning, Molecular</term><term>DNA, Complementary (genetics)</term><term>Fishes (genetics)</term><term>Fishes (growth & development)</term><term>Gene Expression Regulation</term><term>Insulin-Like Growth Factor I (chemistry)</term><term>Insulin-Like Growth Factor I (genetics)</term><term>Insulin-Like Growth Factor I (metabolism)</term><term>Molecular Sequence Data</term><term>Persia</term><term>Phylogeny</term><term>RNA, Messenger (genetics)</term><term>RNA, Messenger (metabolism)</term><term>Sequence Analysis, DNA</term></keywords><keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>Insulin-Like Growth Factor I</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>DNA, Complementary</term><term>Insulin-Like Growth Factor I</term><term>RNA, Messenger</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>RNA, Messenger</term></keywords><keywords scheme="MESH" type="geographic" xml:lang="en"><term>Persia</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Animal Nutritional Physiological Phenomena</term><term>Body Weight</term><term>Fishes</term></keywords><keywords scheme="MESH" qualifier="growth & development" xml:lang="en"><term>Fishes</term></keywords><keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Insulin-Like Growth Factor I</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Amino Acid Sequence</term><term>Animals</term><term>Cloning, Molecular</term><term>Gene Expression Regulation</term><term>Molecular Sequence Data</term><term>Phylogeny</term><term>Sequence Analysis, DNA</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The effects of different periods of starvation (1, 2, 3, and 4 weeks) and subsequent re-feeding (over a 4 week) on the compensatory growth performance and insulin-like growth factor I (IGF-I) mRNA expression in liver and white muscle were investigated in juvenile Persian sturgeon (Acipenser persicus). First, a fragment of 617 nucleotides coding for IGF-I was cloned from liver, which included an open reading frame of 486 nucleotides, encoding a 162 amino acid preproIGF-I. This is composed of a 45 aa for signal peptide, a 117 aa for the mature peptide comprising the B, C, A, and D domains, and a 47 aa for E domain. The mature Persian sturgeon IGF-I exhibits high sequence identities with other sturgeon species and teleost, ranging between 68 and 95 %. The pattern of IGF-I mRNA expression in the liver and white muscle was measured in response to different periods of starvation and subsequent re-feeding. Nutritional status influenced IGF-I mRNA expression pattern in both liver and muscle. IGF-I mRNA expression in the liver increased during starvation, before decreasing after re-feeding. Furthermore, white muscle IGF-I mRNA expression showed better responses to nutritional status and decreased following starvation and increased by re-feeding. However, changes in the expression of IGF-I mRNA were not significantly different between any of the treatments in both tissues. These data suggest that muscle and liver IGF-I mRNA expression do not have a regulatory role for somatic growth induced by compensatory growth in Persain sturgeon.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">24430509</PMID><DateCreated><Year>2014</Year><Month>04</Month><Day>18</Day></DateCreated><DateCompleted><Year>2015</Year><Month>04</Month><Day>06</Day></DateCompleted><DateRevised><Year>2014</Year><Month>04</Month><Day>18</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">2190-3883</ISSN><JournalIssue CitedMedium="Internet"><Volume>55</Volume><Issue>2</Issue><PubDate><Year>2014</Year><Month>May</Month></PubDate></JournalIssue><Title>Journal of applied genetics</Title><ISOAbbreviation>J. Appl. Genet.</ISOAbbreviation></Journal><ArticleTitle>Persian sturgeon insulin-like growth factor I: molecular cloning and expression during various nutritional conditions.</ArticleTitle><Pagination><MedlinePgn>239-47</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1007/s13353-013-0192-7</ELocationID><Abstract><AbstractText>The effects of different periods of starvation (1, 2, 3, and 4 weeks) and subsequent re-feeding (over a 4 week) on the compensatory growth performance and insulin-like growth factor I (IGF-I) mRNA expression in liver and white muscle were investigated in juvenile Persian sturgeon (Acipenser persicus). First, a fragment of 617 nucleotides coding for IGF-I was cloned from liver, which included an open reading frame of 486 nucleotides, encoding a 162 amino acid preproIGF-I. This is composed of a 45 aa for signal peptide, a 117 aa for the mature peptide comprising the B, C, A, and D domains, and a 47 aa for E domain. The mature Persian sturgeon IGF-I exhibits high sequence identities with other sturgeon species and teleost, ranging between 68 and 95 %. The pattern of IGF-I mRNA expression in the liver and white muscle was measured in response to different periods of starvation and subsequent re-feeding. Nutritional status influenced IGF-I mRNA expression pattern in both liver and muscle. IGF-I mRNA expression in the liver increased during starvation, before decreasing after re-feeding. Furthermore, white muscle IGF-I mRNA expression showed better responses to nutritional status and decreased following starvation and increased by re-feeding. However, changes in the expression of IGF-I mRNA were not significantly different between any of the treatments in both tissues. These data suggest that muscle and liver IGF-I mRNA expression do not have a regulatory role for somatic growth induced by compensatory growth in Persain sturgeon.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Yarmohammadi</LastName><ForeName>Mahtab</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>International Sturgeon Research Institute, PO Box: 41635-3464, Rasht, Iran, mahtabyarmohammadi@gmail.com.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Pourkazemi</LastName><ForeName>Mohammad</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Kazemi</LastName><ForeName>Rezvanollah</ForeName><Initials>R</Initials></Author><Author ValidYN="Y"><LastName>Hallajian</LastName><ForeName>Ali</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Soltanloo</LastName><ForeName>Hassan</ForeName><Initials>H</Initials></Author><Author ValidYN="Y"><LastName>Hassanzadeh Saber</LastName><ForeName>Mohammad</ForeName><Initials>M</Initials></Author><Author ValidYN="Y"><LastName>Abbasalizadeh</LastName><ForeName>Alireza</ForeName><Initials>A</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2014</Year><Month>01</Month><Day>16</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>J Appl Genet</MedlineTA><NlmUniqueID>9514582</NlmUniqueID><ISSNLinking>1234-1983</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D018076">DNA, Complementary</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012333">RNA, Messenger</NameOfSubstance></Chemical><Chemical><RegistryNumber>67763-96-6</RegistryNumber><NameOfSubstance UI="D007334">Insulin-Like Growth Factor I</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000595" MajorTopicYN="N">Amino Acid Sequence</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D000824" MajorTopicYN="N">Animal Nutritional Physiological Phenomena</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D001835" MajorTopicYN="N">Body Weight</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003001" MajorTopicYN="N">Cloning, Molecular</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D018076" MajorTopicYN="N">DNA, Complementary</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005399" MajorTopicYN="N">Fishes</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000254" MajorTopicYN="N">growth & development</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D005786" MajorTopicYN="Y">Gene Expression Regulation</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D007334" MajorTopicYN="N">Insulin-Like Growth Factor I</DescriptorName><QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName><QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008969" MajorTopicYN="N">Molecular Sequence Data</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D019071" MajorTopicYN="N" Type="Geographic">Persia</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010802" MajorTopicYN="N">Phylogeny</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012333" MajorTopicYN="N">RNA, Messenger</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017422" MajorTopicYN="N">Sequence Analysis, DNA</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2013</Year><Month>06</Month><Day>30</Day></PubMedPubDate><PubMedPubDate PubStatus="accepted"><Year>2013</Year><Month>12</Month><Day>30</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2013</Year><Month>11</Month><Day>27</Day></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2014</Year><Month>1</Month><Day>17</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="pubmed"><Year>2014</Year><Month>1</Month><Day>17</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2015</Year><Month>4</Month><Day>7</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">24430509</ArticleId><ArticleId IdType="doi">10.1007/s13353-013-0192-7</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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