TY - JOUR
T1 - Gene function analysis by artificial microRNAs in Physcomitrella patens.
AU - Khraiwesh, Basel
AU - Fattash, Isam
AU - Arif, Muhammad Asif
AU - Frank, Wolfgang
N1 - KAUST Repository Item: Exported on 2020-10-01
PY - 2011/4/15
Y1 - 2011/4/15
N2 - MicroRNAs (miRNAs) are ~21 nt long small RNAs transcribed from endogenous MIR genes which form precursor RNAs with a characteristic hairpin structure. miRNAs control the expression of cognate target genes by binding to reverse complementary sequences resulting in cleavage or translational inhibition of the target RNA. Artificial miRNAs (amiRNAs) can be generated by exchanging the miRNA/miRNA sequence of endogenous MIR precursor genes, while maintaining the general pattern of matches and mismatches in the foldback. Thus, for functional gene analysis amiRNAs can be designed to target any gene of interest. During the last decade the moss Physcomitrella patens emerged as a model plant for functional gene analysis based on its unique ability to integrate DNA into the nuclear genome by homologous recombination which allows for the generation of targeted gene knockout mutants. In addition to this, we developed a protocol to express amiRNAs in P. patens that has particular advantages over the generation of knockout mutants and might be used to speed up reverse genetics approaches in this model species.
AB - MicroRNAs (miRNAs) are ~21 nt long small RNAs transcribed from endogenous MIR genes which form precursor RNAs with a characteristic hairpin structure. miRNAs control the expression of cognate target genes by binding to reverse complementary sequences resulting in cleavage or translational inhibition of the target RNA. Artificial miRNAs (amiRNAs) can be generated by exchanging the miRNA/miRNA sequence of endogenous MIR precursor genes, while maintaining the general pattern of matches and mismatches in the foldback. Thus, for functional gene analysis amiRNAs can be designed to target any gene of interest. During the last decade the moss Physcomitrella patens emerged as a model plant for functional gene analysis based on its unique ability to integrate DNA into the nuclear genome by homologous recombination which allows for the generation of targeted gene knockout mutants. In addition to this, we developed a protocol to express amiRNAs in P. patens that has particular advantages over the generation of knockout mutants and might be used to speed up reverse genetics approaches in this model species.
UR - http://hdl.handle.net/10754/561658
UR - http://link.springer.com/10.1007/978-1-61779-123-9_5
UR - http://www.scopus.com/inward/record.url?scp=79961145380&partnerID=8YFLogxK
U2 - 10.1007/978-1-61779-123-9_5
DO - 10.1007/978-1-61779-123-9_5
M3 - Article
C2 - 21533686
SN - 1940-6029
VL - 744
SP - 57
EP - 79
JO - RNAi and Plant Gene Function Analysis
JF - RNAi and Plant Gene Function Analysis
ER -