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大鼠肝脏再生过程中DNA依赖性RNA聚合酶A和B的细胞浓度变化。

Changes in cellular concentration of DNA-dependent RNA polymerases A and B during regeneration of rat liver.

作者信息

Krawczyk Z, Chorazy M

出版信息

Acta Biochim Pol. 1978;25(3):257-71.

PMID:752202
Abstract
  1. DNA-dependent RNA polymerases A and B were solubilized from rat liver nuclei at different intervals after partial hepatectomy, and chromatographed on DEAE-Sephadex A-25. Activity of the solubilized RNA polymerases remained unchanged till 6 h after hepatectomy, then started to increase reaching a maximum (350% and 150% of control for the A and B enzyme, respectively) at the 18th hour of regeneration, and was still high at the 36th hour of regeneration. 2. RNA polymerases A and B were extracted and extensively purified from the nuclei of normal and regenerating rat liver. No marked differences in the specific activities between the analogous purified enzymes from normal and regenerating liver were observed, thus the increase in RNA polymerase activities (especially marked in the case of enzyme A) observed after partial hepatectomy is probably due to a real increase in the quantities of enzymes. 3. Concentration of RNA polymerase A in hepatocyte increases from 1.3 x 10(4) (normal liver) to 7.5 x 10(4) (18 h after hepatectomy) molecules per haploid genome. The concentration of polymerase B increases from 3.4 x 10(4) to 5.5 x 10(4) molecules per haploid genome, respectively.
摘要
  1. 在部分肝切除术后的不同时间间隔,从大鼠肝细胞核中溶解出依赖DNA的RNA聚合酶A和B,并在DEAE-葡聚糖A-25上进行层析。溶解的RNA聚合酶的活性在肝切除术后6小时内保持不变,然后开始增加,在再生的第18小时达到最大值(A酶和B酶分别为对照的350%和150%),并且在再生的第36小时仍然很高。2. 从正常和再生大鼠肝脏的细胞核中提取并广泛纯化RNA聚合酶A和B。未观察到来自正常和再生肝脏的类似纯化酶之间的比活性有明显差异,因此部分肝切除术后观察到的RNA聚合酶活性增加(特别是酶A的情况尤为明显)可能是由于酶量的实际增加。3. 肝细胞中RNA聚合酶A的浓度从每单倍体基因组1.3×10⁴(正常肝脏)增加到7.5×10⁴(肝切除术后18小时)个分子。聚合酶B的浓度分别从每单倍体基因组3.4×10⁴增加到5.5×10⁴个分子。

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