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淋巴细胞激活过程中组蛋白H3组成和合成模式的变化。

Changes in histone H3 composition and synthesis pattern during lymphocyte activation.

作者信息

Wu R S, Tsai S, Bonner W M

出版信息

Biochemistry. 1983 Aug 2;22(16):3868-73. doi: 10.1021/bi00285a023.

Abstract

Freshly isolated human lymphocytes were found to synthesize histones at a significant rate even though no DNA was being synthesized. The synthesis pattern of histone variants in resting lymphocytes is similar to that found in other quiescent cells and different from that found in S-phase cells. For this reason, the histone synthesis in resting lymphocytes cannot be attributed to contamination by S-phase cells. Stimulation by the mitogen phytohemagglutinin resulted in a dramatic switch in the histone H3 variant synthesis pattern as well as a readily apparent change in the histone H3 mass pattern. Thus, the chromatin of activated lymphocytes has a different histone H3 variant composition than resting or quiescent lymphocytes. It is suggested that the proportion of H3.3 in the mass pattern of the chromatin of a cell may be related solely to how long that cell has been quiescent. Inducing resting lymphocytes to synthesize DNA by UV irradiation did not qualitatively change the histone variant synthesis pattern. No S-phase H3 variants were induced by the repair process. Furthermore, the quantity of histone synthesized neither increased nor decreased after treatment with UV light.

摘要

新鲜分离的人淋巴细胞即使在不合成DNA的情况下也能以显著速率合成组蛋白。静息淋巴细胞中组蛋白变体的合成模式与其他静止细胞中的相似,与S期细胞中的不同。因此,静息淋巴细胞中的组蛋白合成不能归因于S期细胞的污染。有丝分裂原植物血凝素的刺激导致组蛋白H3变体合成模式发生显著转变,以及组蛋白H3质量模式出现明显变化。因此,活化淋巴细胞的染色质与静息或静止淋巴细胞具有不同的组蛋白H3变体组成。有人提出,细胞染色质质量模式中H3.3的比例可能仅与该细胞静止的时间长短有关。通过紫外线照射诱导静息淋巴细胞合成DNA并没有定性地改变组蛋白变体合成模式。修复过程未诱导出S期H3变体。此外,紫外线处理后合成的组蛋白数量既没有增加也没有减少。

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