发明名称 МАЛЫЕ МОЛЕКУЛЫ РНК, ОПОСРЕДУЮЩИЕ ИНТЕРФЕРЕНЦИЮ РНК
摘要 Double-stranded RNA (dsRNA) induces sequence-specific post-transcriptional gene silencing in many organisms by a process known as RNA interference (RNAi). Using a Drosophila in vitro system, we demonstrate that 19-23 nt short RNA fragments are the sequence-specific mediators of RNAi. The short interfering RNAs (siRNAs) are generated by an RNase III-like processing reaction from long dsRNA. Chemically synthesized siRNA duplexes with overhanging 3' ends mediate efficient target RNA cleavage in the lysate, and the cleavage site is located near the center of the region spanned by the guiding siRNA. Furthermore, we provide evidence that the direction of dsRNA processing determines whether sense or antisense target RNA can be cleaved by the produced siRNP complex.
申请公布号 RU2007131270(A) 申请公布日期 2009.02.27
申请号 RU20070131270 申请日期 2007.08.16
申请人 МАКС-ПЛАНК-ГЕЗЕЛЛЬШАФТ ЦУР ФЕРДЕРУНГ ДЕР ВИССЕНШАФТЕН Е.Ф. (DE);ОЙРОПЭИШЕС ЛАБОРАТОРИУМ ФЮР МОЛЕКУЛЯРБИОЛОГИ (ЕМБЛ) (DE) 发明人 ТУШЛЬ Томас (DE);ЭЛЬБАШИР Зайда (DE);ЛЕНДЕККЕЛЬ Винфрид (DE);ВИЛЬМ Маттиас (DE)
分类号 A01H5/00;A01K67/027;A61K9/00;A61K31/7105;A61K38/00;A61K45/00;A61K48/00;A61P31/12;A61P35/00;A61P37/02;A61P43/00;C07H;C07H21/00;C12N;C12N1/00;C12N5/10;C12N15/09;C12N15/10;C12N15/113;C12P21/02;C12Q1/02;C12Q1/68;G01N33/15;G01N33/50;G01N33/68 主分类号 A01H5/00
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