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大鼠诱导心肌生长过程中影响DNA合成的核质相互作用。

Nuclear-cytoplasmic interactions affecting DNA synthesis during induced cardiac muscle growth in the rat.

作者信息

Bugaisky L B, Rabinowitz M, Zak R

出版信息

Cardiovasc Res. 1985 Feb;19(2):89-94. doi: 10.1093/cvr/19.2.89.

Abstract

Nuclear-cytoplasmic interactions affecting DNA synthesis during induced cardiac muscle growth were examined in 29 to 46 day old rats. DNA synthesis was examined in vitro using isolated nuclei from rat heart and adult X. laevis spleen. Cytoplasmic extract (CE) was obtained from a 105 000 g supernatant of rat heart and fetal liver homogenates. To measure DNA synthesis we utilised DNA within the isolated quiescent nucleus as the template and measured the effect of CE on the incorporation of 3H-TTP into an acid precipitable product. In a homologous system of rat heart nuclei from weanling rats and CE from cardiac muscle undergoing induced growth, no stimulation of 3H-TTP incorporation was observed. Cardiac muscle CE however, did possess stimulatory factor(s) since quiescent X. laevis nuclei could be stimulated with the rat heart CE. Furthermore, CE from hearts undergoing induced growth had greater activity than extract from control hearts. While cardiac muscle nuclei were not stimulated by heart CE, they showed substantial stimulation by CE from fetal rat liver, which contains a large population of proliferating cells. Stimulation by fetal rat liver was greater with nuclei obtained from hearts undergoing induced growth than from control hearts. Stimulatory factor(s) in CE was distinct from DNA polymerase-alpha activity, as shown by separation of the two activities on a 5 to 15% glycerol gradient.

摘要

在29至46日龄的大鼠中研究了诱导心肌生长过程中影响DNA合成的核质相互作用。使用从大鼠心脏和成年非洲爪蟾脾脏分离的细胞核在体外检测DNA合成。细胞质提取物(CE)从大鼠心脏和胎儿肝脏匀浆的105 000 g上清液中获得。为了测量DNA合成,我们利用分离的静止细胞核内的DNA作为模板,并测量CE对3H-TTP掺入酸沉淀产物的影响。在来自断奶大鼠的大鼠心脏细胞核和来自经历诱导生长的心肌的CE的同源系统中,未观察到3H-TTP掺入的刺激作用。然而,心肌CE确实具有刺激因子,因为静止的非洲爪蟾细胞核可以被大鼠心脏CE刺激。此外,来自经历诱导生长的心脏的CE比来自对照心脏的提取物具有更高的活性。虽然心肌细胞核不受心脏CE的刺激,但它们受到来自含有大量增殖细胞的胎鼠肝脏的CE的显著刺激。与来自对照心脏的细胞核相比,来自经历诱导生长的心脏的细胞核受到胎鼠肝脏的刺激更大。CE中的刺激因子与DNA聚合酶α活性不同,这在5%至15%甘油梯度上对两种活性进行分离时得到了证明。

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