共 66 条
IDENTIFICATION OF CELLULAR PROTEINS THAT CAN INTERACT SPECIFICALLY WITH THE T/E1A-BINDING REGION OF THE RETINOBLASTOMA GENE-PRODUCT
被引:538
作者:

KAELIN, WG
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机构: HARVARD UNIV,SCH MED,BOSTON,MA 02115

PALLAS, DC
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,SCH MED,BOSTON,MA 02115

DECAPRIO, JA
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h-index: 0
机构: HARVARD UNIV,SCH MED,BOSTON,MA 02115

KAYE, FJ
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,SCH MED,BOSTON,MA 02115

LIVINGSTON, DM
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,SCH MED,BOSTON,MA 02115
机构:
[1] HARVARD UNIV,SCH MED,BOSTON,MA 02115
[2] NCI,USN,MED ONCOL BRANCH,BETHESDA,MD 20814
[3] UNIFORMED SERV UNIV HLTH SCI,BETHESDA,MD 20814
来源:
关键词:
D O I:
10.1016/0092-8674(91)90236-R
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The SV40 T antigen (T)/adenovirus E1A-binding domain of the retinoblastoma gene product (pRB) has been fused to S. japonicum glutathione S-transferase, and the chimera, bound to insoluble glutathione, was used to search for cellular proteins that can interact specifically with pRB. At least seven such proteins were detected in extracts of multiple human tumor cell lines. These proteins failed to bind to a family of pRB fusion proteins that harbor inactivating mutations in the T/E1A-binding domain and to the wild-type fusion protein in the presence of a peptide replica of the pRB-binding domain of T. Therefore, the binding of one or more of these proteins may contribute to the growth-suppressing function of pRB.
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页码:521 / 532
页数:12
相关论文
共 66 条
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h-index: 0
机构: WHITEHEAD INST BIOMED RES,CAMBRIDGE,MA 02142

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h-index: 0
机构: WHITEHEAD INST BIOMED RES,CAMBRIDGE,MA 02142

GERBER, MR
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h-index: 0
机构: WHITEHEAD INST BIOMED RES,CAMBRIDGE,MA 02142

HOROWITZ, JM
论文数: 0 引用数: 0
h-index: 0
机构: WHITEHEAD INST BIOMED RES,CAMBRIDGE,MA 02142

FRIEND, SH
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h-index: 0
机构: WHITEHEAD INST BIOMED RES,CAMBRIDGE,MA 02142

SCHARTL, M
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机构: WHITEHEAD INST BIOMED RES,CAMBRIDGE,MA 02142

BOGENMANN, E
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RAPAPORT, JM
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MCGEE, T
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DRYJA, TP
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UNIV CALIF SAN DIEGO,SCH MED,CTR MOLEC GENET,LA JOLLA,CA 92093 UNIV CALIF SAN DIEGO,SCH MED,CTR MOLEC GENET,LA JOLLA,CA 92093
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机构: HARVARD UNIV,SCH MED,DANA FARBER CANC INST,EUKARYOT TRANSCRIPT LAB,BOSTON,MA 02115

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机构: HARVARD UNIV,SCH MED,DANA FARBER CANC INST,EUKARYOT TRANSCRIPT LAB,BOSTON,MA 02115

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机构: HARVARD UNIV,SCH MED,DANA FARBER CANC INST,EUKARYOT TRANSCRIPT LAB,BOSTON,MA 02115
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机构: UNIV UTAH,SCH MED,HOWARD HUGHES MED INST,SALT LAKE CITY,UT 84132

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机构: UNIV UTAH,SCH MED,HOWARD HUGHES MED INST,SALT LAKE CITY,UT 84132

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机构: UNIV UTAH,SCH MED,HOWARD HUGHES MED INST,SALT LAKE CITY,UT 84132

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LUDLOW, JW
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机构: HARVARD UNIV,SCH MED,BOSTON,MA 02115

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机构: HARVARD UNIV,SCH MED,BOSTON,MA 02115

SHEW, JY
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LEE, WH
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MARSILIO, E
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PAUCHA, E
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LUDLOW, JW
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h-index: 0
机构: HARVARD UNIV,SCH MED,BOSTON,MA 02115

LYNCH, D
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,SCH MED,BOSTON,MA 02115

FURUKAWA, Y
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,SCH MED,BOSTON,MA 02115

GRIFFIN, J
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,SCH MED,BOSTON,MA 02115

PIWNICAWORMS, H
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,SCH MED,BOSTON,MA 02115

HUANG, CM
论文数: 0 引用数: 0
h-index: 0
机构: HARVARD UNIV,SCH MED,BOSTON,MA 02115

LIVINGSTON, DM
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h-index: 0
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DUNN, JM
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UNIV TORONTO,DEPT MED GENET,TORONTO M5S 1A8,ONTARIO,CANADA UNIV TORONTO,DEPT MED GENET,TORONTO M5S 1A8,ONTARIO,CANADA

PHILLIPS, RA
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV TORONTO,DEPT MED GENET,TORONTO M5S 1A8,ONTARIO,CANADA UNIV TORONTO,DEPT MED GENET,TORONTO M5S 1A8,ONTARIO,CANADA

BECKER, AJ
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV TORONTO,DEPT MED GENET,TORONTO M5S 1A8,ONTARIO,CANADA UNIV TORONTO,DEPT MED GENET,TORONTO M5S 1A8,ONTARIO,CANADA

GALLIE, BL
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV TORONTO,DEPT MED GENET,TORONTO M5S 1A8,ONTARIO,CANADA UNIV TORONTO,DEPT MED GENET,TORONTO M5S 1A8,ONTARIO,CANADA