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DNA合成抑制对大鼠睾丸中组蛋白合成、周转及沉积的影响。

Effect of inhibition of DNA synthesis on histone synthesis, turnover, and deposition in the rat testis.

作者信息

Chiu M L, Irvin J L

出版信息

Arch Biochem Biophys. 1985 Jan;236(1):260-5. doi: 10.1016/0003-9861(85)90625-3.

Abstract

In testicular seminiferous epithelial cells (SEC) of normal and hypophysectomized rats, 1-beta-D-arabinofuranosylcytosine and hydroxyurea (at concentrations which inhibited DNA synthesis nearly completely) inhibited histone synthesis only partially, and to a different extent for each histone fraction. In the presence of the inhibitors, the extent of synthesis relative to the corresponding control was TH1-x greater than H1 greater than TH2B-x = X2 = H2A greater than H2B = H3 greater than H4, in which synthesis of the H4 fraction was about 50% of control and that of TH1-x was 90-95% of control. The extent of inhibition of synthesis of each histone fraction was similar after hypophysectomy and, therefore, the changing of the relative populations of heterogeneous cells in the SEC did not influence the relative effects of the inhibitors of DNA synthesis on the synthesis of the various histone fractions. After [3H]leucine injection, the molar proportions of labeled histones relative to H4 decreased markedly between 1.5 h and 6-15 days; this finding indicated that there was rapid removal of histones compared to the H4 fraction during this period. When [14C]thymidine was injected 24 h prior to hydroxyurea treatment and [3H]leucine injection, the ratios of specific activities of histone H4 to DNA did not change significantly over an 11-day period. It appears that newly synthesized histone H4 and other somatic histones are associated with existing DNA in the presence of DNA inhibitors.

摘要

在正常大鼠和垂体切除大鼠的睾丸生精上皮细胞(SEC)中,1-β-D-阿拉伯呋喃糖基胞嘧啶和羟基脲(浓度几乎完全抑制DNA合成)仅部分抑制组蛋白合成,且对每个组蛋白组分的抑制程度不同。在抑制剂存在的情况下,相对于相应对照的合成程度为TH1-x>H1>TH2B-x = X2 = H2A>H2B = H3>H4,其中H4组分的合成约为对照的50%,TH1-x的合成约为对照的90 - 95%。垂体切除后,每个组蛋白组分合成的抑制程度相似,因此,SEC中异质细胞相对群体的变化不影响DNA合成抑制剂对各种组蛋白组分合成的相对作用。注射[3H]亮氨酸后,在1.5小时至6 - 15天之间,标记组蛋白相对于H4的摩尔比例显著下降;这一发现表明在此期间与H4组分相比,组蛋白的去除速度很快。当在羟基脲处理和[3H]亮氨酸注射前24小时注射[14C]胸苷时,在11天的时间内组蛋白H4与DNA的比活性没有显著变化。似乎在DNA抑制剂存在的情况下,新合成的组蛋白H4和其他体细胞组蛋白与现有的DNA相关联。

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