Difference between revisions of "IC4R010-miRNA-2010-19796675"

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(The Background of This Project)
(The Background of This Project)
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==The Background of This Project==
 
==The Background of This Project==
*A class of small RNA molecules called microRNAs (miRNAs) has been identified in recent years. MiRNAs are endogenous non-coding
+
*A class of small RNA molecules called microRNAs (miRNAs) has been identified in recent years. MiRNAs are endogenous non-coding RNAs, are 20–22 nucleotides long, and regulate gene expression in eukaryotes ranging from animals to plants [1–6].  
RNAs, are 20–22 nucleotides long, and regulate gene expression in eukaryotes ranging from animals to plants [1–6].  
+
*Four Dicer-like enzymes (DCL1–DCL4) are encoded in the genome of Arabidopsis thaliana [20]. It has been shown that DCL1 is involved in miRNA accumulation [21]. However, there is no dcl1 mutant available for rice. A recent study has shown that the loss of function of OsDCL1 transformants could be used to identify miRNAs[22].
*Four Dicer-like enzymes (DCL1–DCL4) are encoded in the genome of Arabidopsis thaliana [20]. It has been shown that DCL1 is involved in miRNA accumulation [21]. However, there is no dcl1 mutant available for rice. A recent study has shown that the loss of
+
*MiR399 was shown to down-regulate UBC24 mRNA accumulation and to be involved in plant responses to Pi starvation in planta [24,25]. MiR393 has also been shown to inhibit the expression of TIR1 to down-regulated auxin signaling and seedling growth under abiotic stress conditions [4,26]. Moreover, miR159 was shown to involved in hormone signaling and dehydration responses in Arabidopsis [27,28]. However, these observations were all shown in Arabidopsis, few stress-related miRNAs have been discovered in rice.Among miRNAs discovered in rice, only two have been found to be related to abiotic stress, miR393 and miR169g, both up-regulated by dehydration [29].
function of OsDCL1 transformants could be used to identify miRNAs[22].
 
*
 
  
 
==Plant Culture & Treatment==
 
==Plant Culture & Treatment==

Revision as of 12:51, 15 July 2016

Project Title

  • Identification of novel stress-regulated microRNAs from Oryza sativa L.


The Background of This Project

  • A class of small RNA molecules called microRNAs (miRNAs) has been identified in recent years. MiRNAs are endogenous non-coding RNAs, are 20–22 nucleotides long, and regulate gene expression in eukaryotes ranging from animals to plants [1–6].
  • Four Dicer-like enzymes (DCL1–DCL4) are encoded in the genome of Arabidopsis thaliana [20]. It has been shown that DCL1 is involved in miRNA accumulation [21]. However, there is no dcl1 mutant available for rice. A recent study has shown that the loss of function of OsDCL1 transformants could be used to identify miRNAs[22].
  • MiR399 was shown to down-regulate UBC24 mRNA accumulation and to be involved in plant responses to Pi starvation in planta [24,25]. MiR393 has also been shown to inhibit the expression of TIR1 to down-regulated auxin signaling and seedling growth under abiotic stress conditions [4,26]. Moreover, miR159 was shown to involved in hormone signaling and dehydration responses in Arabidopsis [27,28]. However, these observations were all shown in Arabidopsis, few stress-related miRNAs have been discovered in rice.Among miRNAs discovered in rice, only two have been found to be related to abiotic stress, miR393 and miR169g, both up-regulated by dehydration [29].

Plant Culture & Treatment

Research Findings

Labs working on this Project

  • National Centre for Plant Gene Research, Key Laboratory of Molecular and Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences,P.O. Box 2707, South 1-3, Zhongguancun, Beijing 100080, P.R. China
  • State Key Laboratory of Plant Genomics, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, P.R. China
  • National Engineering Research Center for Beijing Biochip Technology, Beijing 102206, China


Corresponding Author

  • Fan Chen:fchen@genetics.ac.cn.