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与扩增的中国仓鼠二氢叶酸还原酶结构域相关的复制起点的分离。

Isolation of the origin of replication associated with the amplified Chinese hamster dihydrofolate reductase domain.

作者信息

Burhans W C, Selegue J E, Heintz N H

出版信息

Proc Natl Acad Sci U S A. 1986 Oct;83(20):7790-4. doi: 10.1073/pnas.83.20.7790.

Abstract

Autoradiography of restriction digests of DNA labeled in early S phase indicates that replication of the amplified dihydrofolate reductase (DHFR) domain of methotrexate-resistant CHOC 400 cells initiates within a 6.1-kilobase pair (kb) EcoRI-doublet located on the 3' side of the DHFR gene. To localize the DHFR origin fragment, synchronized CHOC 400 cells were either pulse labeled with [3H]thymidine in vivo or permeabilized and incubated with [32P]dATP under conditions that support limited chromosomal DNA replication. The temporal order of replication of amplified fragments was determined by hybridization of the in vivo or in vitro replication products to cloned fragments spanning the earliest-replicating portion of the DHFR domain. At the G1/S boundary, the labeled products derived from the replication of amplified sequences, either in whole or permeabilized cells, are distributed about an amplified 4.3-kb Xba I fragment that maps 14 kb downstream from the DHFR gene. As cells progress through the S phase, bidirectional replication away from this site is observed. These studies indicate that the 4.3-kb Xba I fragment contains the origin of replication associated with the amplified DHFR domain.

摘要

对在S期早期标记的DNA限制性酶切片段进行放射自显影表明,耐甲氨蝶呤的CHOC 400细胞中扩增的二氢叶酸还原酶(DHFR)结构域的复制起始于位于DHFR基因3'端的一个6.1千碱基对(kb)的EcoRI双联体内部。为了定位DHFR起始片段,同步化的CHOC 400细胞要么在体内用[3H]胸腺嘧啶脉冲标记,要么在支持有限染色体DNA复制的条件下进行透化处理并用[32P]dATP孵育。通过将体内或体外复制产物与跨越DHFR结构域最早复制部分的克隆片段杂交,确定扩增片段的复制时间顺序。在G1/S边界,来自全细胞或透化细胞中扩增序列复制的标记产物分布在一个扩增的4.3 kb Xba I片段周围,该片段位于DHFR基因下游14 kb处。随着细胞进入S期,观察到从该位点开始的双向复制。这些研究表明,4.3 kb Xba I片段包含与扩增的DHFR结构域相关的复制起点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e11/386807/da8cfe375ef5/pnas00324-0236-a.jpg

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