Grünweller Arnold, Hartmann Roland K
Pharmaceutical Chemistry, Philipps-Universität Marburg, Marbacher Weg 6, Marburg, Germany.
Chembiochem. 2009 Jul 6;10(10):1599-601. doi: 10.1002/cbic.200900271.
Silent partner: In a recent publication, Gunderson and co-workers described an approach to recruit the abundant U1 snRNP, a splicing subparticle, to the last exon of a pre-mRNA, in a sequence-specific manner. This mediates interaction of the U1-70K protein subunit with poly(A) polymerase, thus blocking polyadenylation and inducing pre-mRNA degradation. This novel promising strategy expands the repertoire of gene-silencing concepts.
在最近的一篇出版物中,冈德森及其同事描述了一种方法,可将丰富的U1 snRNP(一种剪接亚颗粒)以序列特异性方式招募到前体mRNA的最后一个外显子上。这介导了U1-70K蛋白亚基与聚腺苷酸聚合酶的相互作用,从而阻断聚腺苷酸化并诱导前体mRNA降解。这种新颖且有前景的策略扩展了基因沉默概念的范畴。