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Adenovirus Small e1a Alters Global Patterns of Histone Modification

机译:小型腺病毒e1a改变组蛋白修饰的整体模式

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Adenovirus small early region la (ela) protein drives cells into S phase by binding RB family proteins and the closely related histone acetyl transferases p300 and CBP. The interaction with RB proteins displaces them from DNA-bound E2F transcription factors, reversing their repression of cell cycle genes. However, it has been unclear how the ela interaction with p300 and CBP promotes passage through the cell cycle. We show that this interaction causes a threefold reduction in total cellular histone H3 lysine 18 acetylation (H3K18ac). CBP and p300 are required for acetylation at this site because their knockdown causes specific hypoacetylation at H3K18. SV40 T antigen also induces H3K18 hypoacetylation. Because global hypoacetylation at this site is observed in prostate carcinomas with poor prognosis, this suggests that processes resulting in global H3K18 hypoacetylation may be linked to oncogenic transformation.
机译:腺病毒小的早期区域la(ela)蛋白通过结合RB家族蛋白和密切相关的组蛋白乙酰基转移酶p300和CBP将细胞驱动到S期。与RB蛋白的相互作用使它们脱离了DNA结合的E2F转录因子,从而逆转了其对细胞周期基因的抑制。但是,尚不清楚与p300和CBP的ela相互作用如何促进细胞周期的传递。我们显示这种相互作用导致总细胞组蛋白H3赖氨酸18乙酰化(H3K18ac)减少三倍。 CBP和p300在此位点需要乙酰化,因为它们的敲低会导致H3K18发生特定的低乙酰化。 SV40 T抗原还诱导H3K18乙酰化不足。因为在预后较差的前列腺癌中观察到该部位的整体乙酰化不足,这表明导致整体H3K18乙酰化不足的过程可能与致癌转化有关。

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