Stabell Marianne, Larsson Jan, Aalen Reidunn B, Lambertsson Andrew
Institute of Molecular Biosciences, University of Oslo, PO Box 1041 Blindern, NO-0316 Oslo, Norway.
Biochem Biophys Res Commun. 2007 Aug 3;359(3):784-9. doi: 10.1016/j.bbrc.2007.05.189. Epub 2007 Jun 4.
Lysine methylation has important functions in biological processes that range from heterochromatin formation to transcription regulation. Here, we demonstrate that Drosophila dSet2 encodes a developmentally essential histone H3 lysine 36 (K36) methyltransferase. Larvae subjected to RNA interference-mediated (RNAi) suppression of dSet2 lack dSet2 expression and H3-K36 methylation, indicating that dSet2 is the sole enzyme responsible for this modification in Drosophila melanogaster. dSet2 RNAi blocks puparium formation and adult development, and causes partial (blister) separation of the dorsal and ventral wing epithelia, defects suggesting a failure of the ecdysone-controlled genetic program. A transheterozygous EcR null mutation/dSet2 RNAi combination produces a complete (balloon) separation of the wing surfaces, revealing a genetic interaction between EcR and dSet2. Using immunoprecipitation, we demonstrate that dSet2 associates with the hyperphosphorylated form of RNA polymerase II (RNAPII).
赖氨酸甲基化在从异染色质形成到转录调控等一系列生物过程中发挥着重要作用。在此,我们证明果蝇dSet2编码一种对发育至关重要的组蛋白H3赖氨酸36(K36)甲基转移酶。经RNA干扰介导(RNAi)抑制dSet2的幼虫缺乏dSet2表达和H3-K36甲基化,这表明dSet2是黑腹果蝇中负责这种修饰的唯一酶。dSet2 RNAi阻断蛹化和成虫发育,并导致背侧和腹侧翅上皮部分(水泡状)分离,这些缺陷表明蜕皮激素控制的遗传程序出现故障。EcR无效突变/dSet2 RNAi的反式杂合组合导致翅表面完全(气球状)分离,揭示了EcR与dSet2之间的遗传相互作用。通过免疫沉淀,我们证明dSet2与RNA聚合酶II(RNAPII)的超磷酸化形式相关联。