INTEGRATION AND TRANSPOSITION OF BACTERIOPHAGE MU
INTEGRATION AND TRANSPOSITION OF BACTERIOPHAGE MU
批准号:
3137993
负责人:
MARTHA M. HOWE
金额:
$10.59万
依托单位国家:
美国
项目类别:
财政年份:
1986
资助国家:
美国
项目状态:
已结题
起止时间:
1986-08-01 至 1987-09-30
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Bacteriophage Mu possesses an unusual recombination system which recognizes
specific attachment sites near the ends of the mature phage DNA and
recombines them with apparently random sequences in the host DHA. The long
range objective of this project is to understand, at the molecular level,
the mechanism by which this recombination occurs. This objective will be
pursued using the following approaches: 1) Studies of lambda phages
containing the ends of Mu will be continued by defining the sites and
functions of Mu which are needed to cause inhibition and lambda::mini-Mu
growth under conditions permissive for Mu gene expression through isolation
and characterization of deletion and point mutant lambda::mini-Mu phages.
New approaches will be tried to isolate the class of lambda::mini-Mu phages
containing the Mu attachment sites close together and to define why these
phages were unstable under previous isolation conditions. 2) The DNA
sequences important for Mu integration will be defined by isolating and
sequencing cis-dominant integration-defective mutants of the
lambda::mini-Mu phage. 3) The relative frequency of cointegrate versus
simple insertion of mini-Mu will be studied to define the role of vector
DNA replication, the effects of Mu lytic versus lysogenic gene expression,
and the roles of specific Mu and host genes in the insertion process.
These studies will significantly advance our knowledge of the sites and
functions involved in Mu integration and the process by which integation
occur. This information is important due to its applicability as a model
for understanding non-homologous recombination processes which are involved
in the spread of antibiotic resistance in bacteria, generation of
spontaneous mutations and DNA rearrangements in procarvotes and eucaryotes,
possible application to directed gene expression and DNA rearrangement
occuring during development in eucaryotes, and the integration of oncogenic
viruses. The fundamental role of such processes in normal and abnormal
growth is now only being recognized and may have great impact in the future.
期刊论文(6)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
Bacteriophage Mu late promoters: four late transcripts initiate near a conserved sequence.
噬菌体 Mu 晚期启动子:四个晚期转录物在保守序列附近起始。
DOI:
10.1128/jb.171.4.2003-2018.1989
发表时间:
1989
期刊:
Journal of bacteriology
影响因子:
3.2
作者:
[Margolin,W, Rao,G, Howe,MM]
通讯作者:
Howe,MM
Characterization of the C operon transcript of bacteriophage Mu.
噬菌体 Mu 的 C 操纵子转录本的表征。
DOI:
10.1128/jb.172.1.361-371.1990
发表时间:
1990
期刊:
Journal of bacteriology
影响因子:
3.2
作者:
[Stoddard,SF, Howe,MM]
通讯作者:
Howe,MM
Bacteriophage Mu sites and functions involved in the inhibition of lambda::mini-Mu growth.
噬菌体 Mu 位点和功能参与抑制 lambda::mini-Mu 生长。
DOI:
10.1016/0042-6822(90)90463-2
发表时间:
1990
期刊:
Virology
影响因子:
3.7
作者:
[Glasgow,AC, Miller,JL, Howe,MM]
通讯作者:
Howe,MM
Activation of the bacteriophage Mu lys promoter by Mu C protein requires the sigma 70 subunit of Escherichia coli RNA polymerase.
Mu C 蛋白激活噬菌体 Mu lys 启动子需要大肠杆菌 RNA 聚合酶的 sigma 70 亚基。
DOI:
10.1128/jb.172.3.1424-1429.1990
发表时间:
1990
期刊:
Journal of bacteriology
影响因子:
3.2
作者:
[Margolin,W, Howe,MM]
通讯作者:
Howe,MM
Frequency of human alloantigen-reactive T lymphocytes. III. Evidence that cyclosporine has an inhibitory effect on human CTL and CTL precursors, independent of CsA-mediated helper T cell dysfunction.
人类同种异体抗原反应性 T 淋巴细胞的频率。
DOI:
--
发表时间:
1988
期刊:
Transplantation
影响因子:
6.2
作者:
[Orosz,CG, Adams,PW, Ferguson,RM]
通讯作者:
Ferguson,RM
ANALYSIS OF INTEGRATION MECHANISM OF BACTERIOPHAGE MU
-
批准号:3125269
-
项目类别:
-
资助金额:$15.04万
-
财政年份:1979
-
负责人:MARTHA M. HOWE
-
依托单位:
ANALYSIS OF INTEGRATION MECHANISM OF BACTERIOPHAGE MU
-
批准号:3125270
-
项目类别:
-
资助金额:$3.85万
-
财政年份:1979
-
负责人:MARTHA M. HOWE
-
依托单位:
海外基金