A resource of vectors and ES cells for targeted deletion of microRNAs in mice.
A resource of vectors and ES cells for targeted deletion of microRNAs in mice.
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DOI:
10.1038/nbt.1929
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发表时间:
2011-08-07
影响因子:
46.9
通讯作者:
Bradley, Allan
中科院分区:
文献类型:
--
作者:
Prosser, Haydn M.;Koike-Yusa, Hiroko;Cooper, James D.;Law, Frances C.;Bradley, Allan
The 21-23 nucleotide single-stranded RNAs classified as microRNAs (miRNA) perform fundamental roles in a wide range of cellular and developmental processes. miRNAs regulate protein expression through sequence-specific base pairing with target messenger RNAs (mRNA) reducing both their stability and the process of protein translation. At least 30% of protein coding genes appear to be conserved targets for miRNAs. In contrast to the protein coding genes, no public resource of miRNA mouse mutant alleles exists. We have generated a library of highly germ-line transmissible C57BL/6N mouse mutant embryonic stem (ES) cells with targeted deletions for the majority of miRNA genes currently annotated within the miRBase registry. These alleles have been designed to be highly adaptable research tools that can be efficiently altered to create reporter, conditional and other allelic variants. This ES cell resource can be searched electronically and is available from ES cell repositories for distribution to the scientific community.
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DOI:
10.1126/science.1139253
发表时间:
2007-04-27
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Rodriguez A;Vigorito E;Clare S;Warren MV;Couttet P;Soond DR;van Dongen S;Grocock RJ;Das PP;Miska EA;Vetrie D;Okkenhaug K;Enright AJ;Dougan G;Turner M;Bradley A
通讯作者:
Bradley A
影响因子:
4.5
作者:
Cai, XZ;Hagedorn, CH;Cullen, BR
通讯作者:
Cullen, BR
影响因子:
14.9
作者:
Griffiths-Jones, S
通讯作者:
Griffiths-Jones, S
影响因子:
64.5
作者:
Marson A;Levine SS;Cole MF;Frampton GM;Brambrink T;Johnstone S;Guenther MG;Johnston WK;Wernig M;Newman J;Calabrese JM;Dennis LM;Volkert TL;Gupta S;Love J;Hannett N;Sharp PA;Bartel DP;Jaenisch R;Young RA
通讯作者:
Young RA
影响因子:
14.9
作者:
Griffiths-Jones S;Grocock RJ;van Dongen S;Bateman A;Enright AJ
通讯作者:
Enright AJ