[Expression of ORIGIN-like sequence in mammalian cells].

Radiobiologiia Pub Date : 1992-11-01
L T Timchenko, V O Fomin, I V Pravosudov, L A Noskin
{"title":"[Expression of ORIGIN-like sequence in mammalian cells].","authors":"L T Timchenko,&nbsp;V O Fomin,&nbsp;I V Pravosudov,&nbsp;L A Noskin","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>There are some genes whose expression increases in non-proliferating hepatocytes after whole-body X-irradiation. We suppose that some of them participate in cell division regulation. To verify our postulate we have studied expression of autonomously replicating sequence pDARC1 in normal, irradiated and dividing rat hepatocytes. We have succeeded earlier in cloning the autonomously replicating sequence pDARC1 and have shown that it could be transcribed in X-irradiated hepatocytes. Here we report on the results of analysis of this sequence expression in dividing mammalian cells. Hybridization with the pDARC1 sequence reveals 4.0 kb mRNA in non-proliferating rat hepatocytes after X-irradiation: this mRNA is absent in normal hepatocytes. Induction of 4.0 kb mRNA is a function of radiation dose; 4.0 kb mRNA content is maximum 6-24 h following whole-body 6 Gy X-irradiation. The 4.0 kb mRNA is also found in dividing rat hepatocytes during the pre-replicative period.</p>","PeriodicalId":20808,"journal":{"name":"Radiobiologiia","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1992-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Radiobiologiia","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

There are some genes whose expression increases in non-proliferating hepatocytes after whole-body X-irradiation. We suppose that some of them participate in cell division regulation. To verify our postulate we have studied expression of autonomously replicating sequence pDARC1 in normal, irradiated and dividing rat hepatocytes. We have succeeded earlier in cloning the autonomously replicating sequence pDARC1 and have shown that it could be transcribed in X-irradiated hepatocytes. Here we report on the results of analysis of this sequence expression in dividing mammalian cells. Hybridization with the pDARC1 sequence reveals 4.0 kb mRNA in non-proliferating rat hepatocytes after X-irradiation: this mRNA is absent in normal hepatocytes. Induction of 4.0 kb mRNA is a function of radiation dose; 4.0 kb mRNA content is maximum 6-24 h following whole-body 6 Gy X-irradiation. The 4.0 kb mRNA is also found in dividing rat hepatocytes during the pre-replicative period.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
ORIGIN-like序列在哺乳动物细胞中的表达
在全身x射线照射后,一些基因在非增殖肝细胞中表达增加。我们认为它们中的一些参与细胞分裂调节。为了验证我们的假设,我们研究了自主复制序列pDARC1在正常、辐照和分裂的大鼠肝细胞中的表达。我们已经成功地克隆了自主复制序列pDARC1,并表明它可以在x射线照射的肝细胞中转录。在这里,我们报告了该序列在哺乳动物细胞分裂中的表达分析结果。与pDARC1序列杂交显示,x射线照射后非增殖大鼠肝细胞中存在4.0 kb mRNA,而正常肝细胞中不存在该mRNA。4.0 kb mRNA的诱导是辐射剂量的函数;全身6 Gy x射线照射后6-24 h, mRNA含量最高达4.0 kb。4.0 kb mRNA也存在于大鼠肝细胞分裂前的复制前期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
[The effect of hematoporphyrin derivative on the postradiation recovery of hemopoiesis in mice]. [The ratio of the contributions from the direct and indirect actions of UV radiation in changing the functional properties of the complement system]. [The effect of irradiation of the thymus, the hypothalamo-hypophyseal area and the gonads on the growth of a transplanted Lewis carcinoma in mice]. [A bacterial model for research on the effect of laser radiation on the intensity of cell division]. [The functional activity of the hypothalamo-hypophyseal-gonadal system in male rats in the late periods after x-ray irradiation].
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1