dna的生物合成和损伤修复dna biosynthesis and dna damage repa

上传人:tia****nde 文档编号:71365261 上传时间:2019-01-20 格式:PPT 页数:100 大小:403.81KB
返回 下载 相关 举报
dna的生物合成和损伤修复dna biosynthesis and dna damage repa_第1页
第1页 / 共100页
dna的生物合成和损伤修复dna biosynthesis and dna damage repa_第2页
第2页 / 共100页
dna的生物合成和损伤修复dna biosynthesis and dna damage repa_第3页
第3页 / 共100页
dna的生物合成和损伤修复dna biosynthesis and dna damage repa_第4页
第4页 / 共100页
dna的生物合成和损伤修复dna biosynthesis and dna damage repa_第5页
第5页 / 共100页
点击查看更多>>
资源描述

《dna的生物合成和损伤修复dna biosynthesis and dna damage repa》由会员分享,可在线阅读,更多相关《dna的生物合成和损伤修复dna biosynthesis and dna damage repa(100页珍藏版)》请在金锄头文库上搜索。

1、Chapter 15 DNA Biosynthesis and DNA Damage Repair,Section One The General Features of Replication of Chromosomal DNA,DNA replicates semiconservatively. . Watson and Crick predicted that DNA might semiconservatively replicate.,the hypothesis _ p _ d _ p _ p _ d _ p,. In 1958 Meselson and Stahl demons

2、- trated the semiconservative nature of DNA replication in E coli.,The experiment: CsCl equilibrium gradient density ultracentri- fugation of 15N labeled E coli DNA.,The density of DNA was increased by labeling it with 15N, a heavy isotope of nitrogen. This was done by growing E coli 15 ge- neration

3、s in a medium that contained 15NH4Cl as its only nitrogen source.,15N DNA was extracted and subjected to CsCl equilibrium gradient density ultracen- trifugation. The DNA band position was recorded. There was one band of 15N DNA.,The bacteria were transferred to an 14NH4Cl medium and grown for one ge

4、neration. The DNA density was determined again. The position of the DNA band was compared with that of the 15N DNA .,What was the result ?,There was one DNA band. It had a lower density than 15N DNA because its position was above on that of 15N DNA. It was 15N/14N hybrid DNA.,After another generatio

5、n growing in the 14NH4Cl medium the bacterial DNA density was determined. There were two DNA bands.,One half of the DNA was 14N DNA, and another half was hybrid DNA. In succeeding generations the ratio of 14N DNA to hybrid DNA increased gradually. The hybrid DNA became less and less,summary DNA repl

6、icates in a semiconservative man- ner. When the two parental strands sepa- rate, each serves as the template for making a new , complementary strand.,2. The point at which separation of the strands and synthesis of new DNA takes place is known as the replication fork. The replication fork is Y-shape

7、d. Two arms (V) are separated strands which act as the template and DNA synthesis is actively taking place. The body (I) is the parental DNA.,3.DNA replication is usually bidirectional. .Replicon: Any piece which replicates as a single unit is called a replicon. All bacterial chromosomes and many ph

8、age and virus DNA molecules are circular and comprise single replicons.,In contrast eukaryotic chromosomes consist of multiple replicons. . Origin: The initiation within a replicon always occurs at a fixed point known as the origin.,.Terminus: In a circular replicon there is a single termination sit

9、e roughly 180 opposite the unique origin.,Summary In a circular replicon replication begins from the fixed origin and forms two repli-cation forks. The two replication forks proceed bidirec- tionally away from the origin and the strands are copied as they separate until the terminus is reached.,4. D

10、NA replication is semidiscontinuous. .The mechanism of DNA replication allows only for synthesis in a 53 direction. . The two strands of DNA are antiparallel.,Question How is the parental strand that runs 53 past the replication fork copied ? The answer is semidiscontinuous replica- tion.,At each re

11、plication fork one strand ( the lead- ing strand ), whose template runs 35 past the replication fork, is synthesized as one con- tinuous piece, while the other strand ( the lag- ging strand ), whose template runs 53 past the replication fork is made discontinuously as short fragments in the reverse

12、direction.,These short fragments are called Okazaki fragments. They are joined by DNA ligase and form the lagging strand.,5. Origins contain short AT-rich repeat se- quences. . Prokaryotic and eukaryotic origins have common features: a. They consist of multiple unique short repeat sequences. b. Thes

13、e sequences are recognition and binding sites of multi-subunit initiation factors.,c. These sequences are usually AT- rich. . E coli s origin is called oriC. It is 254bp long and contains three 13-bp direct repeats and four 9-bp inverted re- peats.,6. DNA replication needs priming. . DNA polymerases

14、 cannot initiate DNA replication by starting a new DNA chain. They can only add nucleotides to the 3 end of an existent piece of RNA or DNA under the direction of the template. The existent piece of RNA or DNA are called primer.,. The leading strand and all Okazaki frag- ments are primed by synthesi

15、s of a short piece of RNA ( an RNA primer ), which is then elongated with DNA by DNA poly- merase. . There are also DNA priming or nucleotide priming.,7.Multi-enzymes and proteins participate in DNA replication. . Topoisomerases regulate the type and level of supercoiling of dsDNA. . Helicases unwin

16、d the dsDNA. . SSBs bind and stabilize the single DNA strand. . Primase synthesizes the RNA primer.,. DNA polymerases elongate DNA chains. . DNA ligase joins Okazaki fragments.,8. DNA replication is of high fidelity. . There are two types of replication errors. a. base ( nucleotide ) substitution. b. nucleotide insertion or deletion. . There are two types of error controls a. presynthetic e

展开阅读全文
相关资源
相关搜索

当前位置:首页 > 高等教育 > 大学课件

电脑版 |金锄头文库版权所有
经营许可证:蜀ICP备13022795号 | 川公网安备 51140202000112号