Systematic analysis of palatal transcriptome to identify cleft palate genes within TGFβ3-knockout mice alleles: RNA-Seq analysis of TGFβ3 Mice
Identifieur interne : 005628 ( Ncbi/Checkpoint ); précédent : 005627; suivant : 005629Systematic analysis of palatal transcriptome to identify cleft palate genes within TGFβ3-knockout mice alleles: RNA-Seq analysis of TGFβ3 Mice
Auteurs : Ferhat Ozturk [États-Unis, Turquie] ; You Li [États-Unis] ; Xiujuan Zhu [États-Unis] ; Chittibabu Guda [États-Unis] ; Ali Nawshad [États-Unis]Source :
- BMC Genomics [ 1471-2164 ] ; 2013.
Abstract
In humans, cleft palate (CP) accounts for one of the largest number of birth defects with a complex genetic and environmental etiology. TGFβ3 has been established as an important regulator of palatal fusion in mice and it has been shown that TGFβ3-null mice exhibit CP without any other major deformities. However, the genes that regulate cellular decisions and molecular mechanisms maintained by the TGFβ3 pathway throughout palatogenesis are predominantly unexplored. Our objective in this study was to analyze global transcriptome changes within the palate during different gestational ages within TGFβ3 knockout mice to identify TGFβ3-associated genes previously unknown to be associated with the development of cleft palate. We used deep sequencing technology, RNA-Seq, to analyze the transcriptome of TGFβ3 knockout mice at crucial stages of palatogenesis, including palatal growth (E14.5), adhesion (E15.5), and fusion (E16.5).
The overall transcriptome analysis of TGFβ3 wildtype mice (C57BL/6) reveals that almost 6000 genes were upregulated during the transition from E14.5 to E15.5 and more than 2000 were downregulated from E15.5 to E16.5. Using bioinformatics tools and databases, we identified the most comprehensive list of CP genes (n = 322) in which mutations cause CP either in humans or mice, and analyzed their expression patterns. The expression motifs of CP genes between TGFβ3+/− and TGFβ3−/− were not significantly different from each other, and the expression of the majority of CP genes remained unchanged from E14.5 to E16.5. Using these patterns, we identified 8 unique genes within TGFβ3−/− mice (
Our study represents the first analysis of the palatal transcriptome of the mouse, as well as TGFβ3 knockout mice, using deep sequencing methods. In this study, we characterized the critical regulation of palatal transcripts that may play key regulatory roles through crucial stages of palatal development. We identified potential causative CP genes in a TGFβ3 knockout model, which may lead to a better understanding of the genetic mechanisms of palatogenesis and provide novel potential targets for gene therapy approaches to treat cleft palate.
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DOI: 10.1186/1471-2164-14-113
PubMed: 23421592
PubMed Central: 3618314
Affiliations:
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Systematic analysis of palatal transcriptome to identify cleft palate genes within TGFβ3-knockout mice alleles: RNA-Seq analysis of TGFβ3 Mice</title><author><name sortKey="Ozturk, Ferhat" sort="Ozturk, Ferhat" uniqKey="Ozturk F" first="Ferhat" last="Ozturk">Ferhat Ozturk</name><affiliation wicri:level="1"><nlm:aff id="I1">Department of Oral Biology, College of Dentistry, University of Nebraska Medical Center, 40th and Holdrege St, Lincoln, NE 68583, USA</nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Oral Biology, College of Dentistry, University of Nebraska Medical Center, 40th and Holdrege St, Lincoln, NE 68583</wicri:regionArea><wicri:noRegion>NE 68583</wicri:noRegion></affiliation><affiliation wicri:level="1"><nlm:aff id="I4">Current address: Department of Molecular Biology and Genetics, Canik Basari University Canik, Samsun 55080, Turkey</nlm:aff><country xml:lang="fr">Turquie</country><wicri:regionArea>Current address: Department of Molecular Biology and Genetics, Canik Basari University Canik, Samsun 55080</wicri:regionArea><wicri:noRegion>Samsun 55080</wicri:noRegion></affiliation></author><author><name sortKey="Li, You" sort="Li, You" uniqKey="Li Y" first="You" last="Li">You Li</name><affiliation wicri:level="1"><nlm:aff id="I2">Department of Genetics and Cell Biology, University of Nebraska Medical Center, Omaha, NE, USA</nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Genetics and Cell Biology, University of Nebraska Medical Center, Omaha, NE</wicri:regionArea><wicri:noRegion>NE</wicri:noRegion></affiliation></author><author><name sortKey="Zhu, Xiujuan" sort="Zhu, Xiujuan" uniqKey="Zhu X" first="Xiujuan" last="Zhu">Xiujuan Zhu</name><affiliation wicri:level="1"><nlm:aff id="I1">Department of Oral Biology, College of Dentistry, University of Nebraska Medical Center, 40th and Holdrege St, Lincoln, 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Mice</title><author><name sortKey="Ozturk, Ferhat" sort="Ozturk, Ferhat" uniqKey="Ozturk F" first="Ferhat" last="Ozturk">Ferhat Ozturk</name><affiliation wicri:level="1"><nlm:aff id="I1">Department of Oral Biology, College of Dentistry, University of Nebraska Medical Center, 40th and Holdrege St, Lincoln, NE 68583, USA</nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Oral Biology, College of Dentistry, University of Nebraska Medical Center, 40th and Holdrege St, Lincoln, NE 68583</wicri:regionArea><wicri:noRegion>NE 68583</wicri:noRegion></affiliation><affiliation wicri:level="1"><nlm:aff id="I4">Current address: Department of Molecular Biology and Genetics, Canik Basari University Canik, Samsun 55080, Turkey</nlm:aff><country xml:lang="fr">Turquie</country><wicri:regionArea>Current address: Department of Molecular Biology and Genetics, Canik Basari University Canik, Samsun 55080</wicri:regionArea><wicri:noRegion>Samsun 55080</wicri:noRegion></affiliation></author><author><name sortKey="Li, You" sort="Li, You" uniqKey="Li Y" first="You" last="Li">You Li</name><affiliation wicri:level="1"><nlm:aff id="I2">Department of Genetics and Cell Biology, University of Nebraska Medical Center, Omaha, NE, USA</nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Genetics and Cell Biology, University of Nebraska Medical Center, Omaha, NE</wicri:regionArea><wicri:noRegion>NE</wicri:noRegion></affiliation></author><author><name sortKey="Zhu, Xiujuan" sort="Zhu, Xiujuan" uniqKey="Zhu X" first="Xiujuan" last="Zhu">Xiujuan Zhu</name><affiliation wicri:level="1"><nlm:aff id="I1">Department of Oral Biology, College of Dentistry, University of Nebraska Medical Center, 40th and Holdrege St, Lincoln, NE 68583, USA</nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Oral Biology, College of Dentistry, University of Nebraska Medical Center, 40th and Holdrege St, Lincoln, NE 68583</wicri:regionArea><wicri:noRegion>NE 68583</wicri:noRegion></affiliation></author><author><name sortKey="Guda, Chittibabu" sort="Guda, Chittibabu" uniqKey="Guda C" first="Chittibabu" last="Guda">Chittibabu Guda</name><affiliation wicri:level="1"><nlm:aff id="I2">Department of Genetics and Cell Biology, University of Nebraska Medical Center, Omaha, NE, USA</nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Genetics and Cell Biology, University of Nebraska Medical Center, Omaha, NE</wicri:regionArea><wicri:noRegion>NE</wicri:noRegion></affiliation><affiliation wicri:level="1"><nlm:aff id="I3">Bioinformatics and Systems Biology Core Facility, University of Nebraska Medical Center, Omaha, NE, USA</nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea>Bioinformatics and Systems Biology Core Facility, University of Nebraska Medical Center, Omaha, NE</wicri:regionArea><wicri:noRegion>NE</wicri:noRegion></affiliation></author><author><name sortKey="Nawshad, Ali" sort="Nawshad, Ali" uniqKey="Nawshad A" first="Ali" last="Nawshad">Ali Nawshad</name><affiliation wicri:level="1"><nlm:aff id="I1">Department of Oral Biology, College of Dentistry, University of Nebraska Medical Center, 40th and Holdrege St, Lincoln, NE 68583, USA</nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Oral Biology, College of Dentistry, University of Nebraska Medical Center, 40th and Holdrege St, Lincoln, NE 68583</wicri:regionArea><wicri:noRegion>NE 68583</wicri:noRegion></affiliation></author></analytic><series><title level="j">BMC Genomics</title><idno type="eISSN">1471-2164</idno><imprint><date when="2013">2013</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><sec><title>Background</title><p>In humans, cleft palate (CP) accounts for one of the largest number of birth defects with a complex genetic and environmental etiology. TGFβ3 has been established as an important regulator of palatal fusion in mice and it has been shown that TGFβ3-null mice exhibit CP without any other major deformities. However, the genes that regulate cellular decisions and molecular mechanisms maintained by the TGFβ3 pathway throughout palatogenesis are predominantly unexplored. Our objective in this study was to analyze global transcriptome changes within the palate during different gestational ages within TGFβ3 knockout mice to identify TGFβ3-associated genes previously unknown to be associated with the development of cleft palate. We used deep sequencing technology, RNA-Seq, to analyze the transcriptome of TGFβ3 knockout mice at crucial stages of palatogenesis, including palatal growth (E14.5), adhesion (E15.5), and fusion (E16.5).</p></sec><sec><title>Results</title><p>The overall transcriptome analysis of TGFβ3 wildtype mice (C57BL/6) reveals that almost 6000 genes were upregulated during the transition from E14.5 to E15.5 and more than 2000 were downregulated from E15.5 to E16.5. Using bioinformatics tools and databases, we identified the most comprehensive list of CP genes (n = 322) in which mutations cause CP either in humans or mice, and analyzed their expression patterns. The expression motifs of CP genes between TGFβ3+/− and TGFβ3−/− were not significantly different from each other, and the expression of the majority of CP genes remained unchanged from E14.5 to E16.5. Using these patterns, we identified 8 unique genes within TGFβ3−/− mice (<italic>Chrng, Foxc2, H19, Kcnj13, Lhx8, Meox2, Shh,</italic> and <italic>Six3)</italic>, which may function as the primary contributors to the development of cleft palate in TGFβ3−/− mice. When the significantly altered CP genes were overlaid with TGFβ signaling, all of these genes followed the Smad-dependent pathway.</p></sec><sec><title>Conclusions</title><p>Our study represents the first analysis of the palatal transcriptome of the mouse, as well as TGFβ3 knockout mice, using deep sequencing methods. In this study, we characterized the critical regulation of palatal transcripts that may play key regulatory roles through crucial stages of palatal development. We identified potential causative CP genes in a TGFβ3 knockout model, which may lead to a better understanding of the genetic mechanisms of palatogenesis and provide novel potential targets for gene therapy approaches to treat cleft palate.</p></sec></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Schutte, Bc" uniqKey="Schutte B">BC Schutte</name></author><author><name sortKey="Murray, Jc" uniqKey="Murray J">JC Murray</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Nawshad, A" uniqKey="Nawshad A">A Nawshad</name></author><author><name sortKey="Hay, Ed" uniqKey="Hay E">ED Hay</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Nawshad, A" uniqKey="Nawshad A">A Nawshad</name></author><author><name sortKey="Lagamba, D" uniqKey="Lagamba D">D LaGamba</name></author><author><name sortKey="Olsen, Br" uniqKey="Olsen B">BR Olsen</name></author><author><name sortKey="Hay, Ed" 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Chetvernin</name></author><author><name sortKey="Church, Dm" uniqKey="Church D">DM Church</name></author><author><name sortKey="Dicuccio, M" uniqKey="Dicuccio M">M DiCuccio</name></author><author><name sortKey="Edgar, R" uniqKey="Edgar R">R Edgar</name></author><author><name sortKey="Federhen, S" uniqKey="Federhen S">S Federhen</name></author></analytic></biblStruct></listBibl></div1></back></TEI><affiliations><list><country><li>Turquie</li><li>États-Unis</li></country></list><tree><country name="États-Unis"><noRegion><name sortKey="Ozturk, Ferhat" sort="Ozturk, Ferhat" uniqKey="Ozturk F" first="Ferhat" last="Ozturk">Ferhat Ozturk</name></noRegion><name sortKey="Guda, Chittibabu" sort="Guda, Chittibabu" uniqKey="Guda C" first="Chittibabu" last="Guda">Chittibabu Guda</name><name sortKey="Guda, Chittibabu" sort="Guda, Chittibabu" uniqKey="Guda C" first="Chittibabu" last="Guda">Chittibabu Guda</name><name sortKey="Li, You" sort="Li, You" uniqKey="Li Y" first="You" last="Li">You Li</name><name sortKey="Nawshad, Ali" sort="Nawshad, Ali" uniqKey="Nawshad A" first="Ali" last="Nawshad">Ali Nawshad</name><name sortKey="Zhu, Xiujuan" sort="Zhu, Xiujuan" uniqKey="Zhu X" first="Xiujuan" last="Zhu">Xiujuan Zhu</name></country><country name="Turquie"><noRegion><name sortKey="Ozturk, Ferhat" sort="Ozturk, Ferhat" uniqKey="Ozturk F" first="Ferhat" last="Ozturk">Ferhat Ozturk</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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