CLONING & CHARACTER OF C-MYC PROMOTER BINDING PROTEIN
CLONING & CHARACTER OF C-MYC PROMOTER BINDING PROTEIN
批准号:
3459970
负责人:
Ratna B. Ray
金额:
$6.13万
依托单位国家:
美国
项目类别:
财政年份:
1991
资助国家:
美国
项目状态:
已结题
起止时间:
1991-09-30 至 1993-08-31
关键词:
DNA binding protein HeLa cells antisense nucleic acid cell growth regulation complementary DNA gene expression genetic promoter element genetic recombination genetic regulatory element immunofluorescence technique molecular cloning nucleic acid sequence protooncogene site directed mutagenesis transfection
中文摘要
c-myc原癌基因在调节
英文摘要
The c-myc protooncogene plays an important role in the regulation of
cellular growth and proliferation. Expression of this important gene is
regulated by a number of external stimuli in malignant and nonmalignant
cells. We have shown that c-myc expression is selectively inhibited by the
G-C specific DNA binding drugs mithramycin. Using this approach we have
identified G-C rich sequences located 5' of the P1 and P2 c-myc promoters
which bind putative regulator factors. The G-C rich P1 region binds the
Sp1 regulatory protein but with G-C rich P2 region does not. We have used
double stranded oligonucleotides to the P2 regulatory region to screen a
cDNA expression library and have identified and characterized a gene which
encodes a protein binding to this region. This proposal will test the
hypothesis that the c-myc promoter binding protein (MBP-1) is a c-myc
regulatory protein and that it plays an important role in the regulation of
c-myc expression. A second c-myc promoter binding protein, MBP-2, which
binds to the ME1a2 region of the P2 promoter, has also been identified.
Its role in the regulation of c-myc expression will also be characterized.
The specific aims of this proposal are:
1. To investigate the role of the MBP-1 and MBP-2 proteins in the
regulation of the c-myc promoter activity.
2. To characterize the role of MBP-1 and MBP-2 in the regulation of
cellular proliferation.
3. To sequence the MBP-2 gene and to characterize its interaction with the
c-myc promoter sequence.
4. To purify and characterize the recombinant and naturally occurring
protein products of the MBP-1 and MBP-2 genes and determine their cellular
localization.
These studies will provide important new information about the regulation
of the c-myc protooncogene and will allow us to determine the role of the
c-myc promoter binding protein as a putative myc regulatory protein.
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