Senatore B, Cafieri A, Di Marino I, Rosati M, Di Nocera P P, Grimaldi G
International Institute of Genetics and Biophysics, CNR, Via Marconi 10, Naples, Italy.
Gene. 1999 Jul 8;234(2):381-94. doi: 10.1016/s0378-1119(99)00182-1.
KRAB/FPB (Krüppel-associated/finger preceding box) domains are small, portable transcriptional repression motifs, encoded by hundreds of vertebrates C2-H2-type zinc finger genes. We report that KRAB/FPB domains feature an unprecedented, highly promiscuous DNA-binding dependent transcriptional repressing activity. Indeed, template bound chimeric factors containing KRAB/FPB modules actively repress in vivo the transcription of distinct promoter classes that depend on different core elements, recruit distinct basal transcriptional apparatuses and are transcribed either by RNA polymerase II or III. The promoter types repressed in transient assays in a dose- and DNA-binding dependent, but position- and orientation-independent manner, by GAL4-KRAB/FPB fusions include an RNA polymerase II-dependent small nuclear RNA promoter (U1) as well as RNA polymerase III-dependent class 2 (adenovirus VA1), class 3 (human U6) and atypical (human 7SL) promoters. Down-modulation of all of these templates depended on factors containing the A module of the KRAB/FPB domain. Data provide further insights into the properties and mode of action of this widespread repression motif, and support the notion that genes belonging to distinct classes may be repressed in vivo by KRAB/FPB containing zinc finger proteins. The exquisitely DNA-binding dependent transcriptional promiscuity exhibited by KRAB/FPB domains may provide a unique model system for studying the mechanism by which a promoter recruited repression motif can down-modulate a large variety of promoter types.
KRAB/FPB(与Krüppel相关/前框指)结构域是小型的、可移植的转录抑制基序,由数百个脊椎动物C2-H2型锌指基因编码。我们报告称,KRAB/FPB结构域具有前所未有的、高度混杂的依赖DNA结合的转录抑制活性。实际上,包含KRAB/FPB模块的模板结合嵌合因子在体内能有效抑制不同启动子类别的转录,这些启动子依赖不同的核心元件,招募不同的基础转录装置,并由RNA聚合酶II或III转录。在瞬时分析中,GAL4-KRAB/FPB融合蛋白以剂量和DNA结合依赖但位置和方向独立的方式抑制的启动子类型包括RNA聚合酶II依赖的小核RNA启动子(U1)以及RNA聚合酶III依赖的2类(腺病毒VA1)、3类(人U6)和非典型(人7SL)启动子。所有这些模板的下调都依赖于包含KRAB/FPB结构域A模块的因子。这些数据进一步揭示了这种广泛存在的抑制基序的特性和作用模式,并支持这样一种观点,即属于不同类别的基因在体内可能被含KRAB/FPB的锌指蛋白所抑制。KRAB/FPB结构域所展现出的对DNA结合高度依赖的转录混杂性,可能为研究启动子招募的抑制基序下调多种启动子类型的机制提供一个独特的模型系统。