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   <subfield code="a">10.1007/s00425-015-2287-3</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/s00425-015-2287-3</subfield>
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   <subfield code="a">Association mapping in Populus reveals the interaction between Pto - miR530a and its target Pto - KNAT1</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Xiaohui Yang, Qingzhang Du, Jinhui Chen, Bowen Wang, Deqiang Zhang]</subfield>
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   <subfield code="a">Main conclusion : We used transcript profiling and multi-SNP association to investigate the genetic regulatory relationship between miRNA Pto-miR530a and its target Pto-KNAT1, identifying additive, dominant, and epistatic effects. MicroRNAs (miRNAs) play crucial roles in the post-transcriptional regulation of plant growth and development; indeed, many studies have described the importance of miRNA-target interactions in herbaceous species. However, elucidation of the miRNA-target interactions in trees may require novel strategies. In the present study, we describe a strategy combining expression profiling by reverse transcription quantitative PCR (RT-qPCR) and association mapping with multiple single nucleotide polymorphisms (SNPs) to evaluate the interaction between Pto-miR530a and its target Pto-KNAT1 in Populus tomentosa. RT-qPCR analysis showed a negative correlation (r=−0.62, P&lt;0.05) between expression levels of Pto-miR530a and Pto-KNAT1 in eight tissues. We used a Bayesian hierarchical model to identify allelic variants of Pto-miR530a and Pto-KNAT1 that associated with eight traits related to growth and wood properties, in a population of 460 unrelated individuals of P. tomentosa. This analysis identified 27 associations, with the proportions of phenotypic variance (R 2) contributed by each SNP ranging of 0.82-15.81%, the additive effects of each SNP ranging of 0.16-18.09, and the dominant effects ranging from −14.09 to 19.00. Epistatic interaction models showed a strong interaction among SNPs in the miRNA target with R 2 of 0.1-3.56%, and information gain of significant SNP pairs of −3.09 to 0.93%, representing the regulatory interactions between the miRNA and the mRNA. Thus, we used a new strategy that combines association genetics and expression profiling based on SNPs to study the regulatory relationship between this miRNA and its target mRNA, thereby providing novel advances in our understanding of the genetic architecture of important traits.</subfield>
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   <subfield code="a">Springer-Verlag Berlin Heidelberg, 2015</subfield>
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   <subfield code="a">Association genetics</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Epistasis</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">MiRNA/target interaction</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Transcript profiling</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Tree growth</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">Wood properties</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">5′-UTR : 5′-untranslated region</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">DBH : Diameter at breast height</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">FL : Fiber length</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">FW : Fiber width</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">fGWAS : Functional genome-wide association studies</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">HC : Holocellulose content</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">IG : Information gain</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">LC : Lignin content</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">LD : Linkage disequilibrium</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">MFA : Microfiber angle</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">miRNAs : MicroRNAs</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">MDR3.0.2 : Multifactor dimensionality reduction 3.0.2</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">PCN : POPCORONA</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">PCA : Principle component analysis</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">RT-qPCR : Reverse transcription quantitative PCR</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">SNP : Single nucleotide polymorphism</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">V : Stem volume</subfield>
   <subfield code="2">nationallicence</subfield>
  </datafield>
  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">H : Tree height</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Yang</subfield>
   <subfield code="D">Xiaohui</subfield>
   <subfield code="u">National Engineering Laboratory for Tree Breeding, College of Biological Sciences and Technology, Beijing Forestry University, No. 35, Qinghua East Road, 100083, Beijing, People's Republic of China</subfield>
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   <subfield code="a">Du</subfield>
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   <subfield code="u">National Engineering Laboratory for Tree Breeding, College of Biological Sciences and Technology, Beijing Forestry University, No. 35, Qinghua East Road, 100083, Beijing, People's Republic of China</subfield>
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   <subfield code="a">Chen</subfield>
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   <subfield code="a">Wang</subfield>
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   <subfield code="a">Zhang</subfield>
   <subfield code="D">Deqiang</subfield>
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   <subfield code="t">Planta</subfield>
   <subfield code="d">Springer Berlin Heidelberg</subfield>
   <subfield code="g">242/1(2015-07-01), 77-95</subfield>
   <subfield code="x">0032-0935</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="D">1</subfield>
   <subfield code="a">research-article</subfield>
   <subfield code="2">jats</subfield>
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