A unique domain of pRb2/p130 acts as an inhibitor of Cdk2 kinase activity

被引:75
作者
DeLuca, A
MacLachlan, TK
Bagella, L
Dean, C
Howard, CM
Claudio, PP
Baldi, A
Khalili, K
Giordano, A
机构
[1] THOMAS JEFFERSON UNIV,JEFFERSON MED COLL,DEPT PATHOL,PHILADELPHIA,PA 19107
[2] THOMAS JEFFERSON UNIV,JEFFERSON MED COLL,DEPT ANAT & CELL BIOL,PHILADELPHIA,PA 19107
[3] THOMAS JEFFERSON UNIV,JEFFERSON MED COLL,SBARRO INST CANC RES & MOL MED,PHILADELPHIA,PA 19107
[4] THOMAS JEFFERSON UNIV,JEFFERSON INST MOL MED,DEPT BIOCHEM & MOL BIOL,PHILADELPHIA,PA 19107
关键词
D O I
10.1074/jbc.272.34.20971
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 Cdk2 kinase has long been known to be involved in the progression of mammalian cells past the G(1) phase restriction point and through DNA replication in the cell cycle. The Rb family of proteins, consisting of pRb, p107, and pRb2/p130, has also been shown to monitor progression of G, phase, mostly through their interaction with E2F family members. p107 is able to inhibit Cdk2 kinase activity through this interaction via a p21-related domain present in the C terminus of the protein. We show here that pRb2/p130 also possesses this activity, but through a separate domain. Moreover, we correlate the increased expression of pRb2/p130 during various cellular processes with the decreased kinase activity of Cdk2. We hypothesize that pRb2/p130 may act not only to bind and modify E2F activity, but also to inhibit Cdk2 kinase activity in concert with p21 in a manner different from p107.
引用
收藏
页码:20971 / 20974
页数:4
相关论文
共 21 条
  • [1] THE RB2/P130 GENE-PRODUCT IS A NUCLEAR-PROTEIN WHOSE PHOSPHORYLATION IS CELL-CYCLE-REGULATED
    BALDI, A
    DELUCA, A
    CLAUDIO, PP
    BALDI, F
    GIORDANO, GG
    TOMMASINO, M
    PAGGI, MG
    GIORDANO, A
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 1995, 59 (03) : 402 - 408
  • [2] BUCK V, 1995, ONCOGENE, V11, P31
  • [3] THE E2F TRANSCRIPTION FACTOR IS A CELLULAR TARGET FOR THE RB PROTEIN
    CHELLAPPAN, SP
    HIEBERT, S
    MUDRYJ, M
    HOROWITZ, JM
    NEVINS, JR
    [J]. CELL, 1991, 65 (06) : 1053 - 1061
  • [4] Claudio PP, 1996, CANCER RES, V56, P2003
  • [5] A NEW HUMAN P34 PROTEIN-KINASE, CDK2, IDENTIFIED BY COMPLEMENTATION OF A CDC28 MUTATION IN SACCHAROMYCES-CEREVISIAE, IS A HOMOLOG OF XENOPUS-EG1
    ELLEDGE, SJ
    SPOTTSWOOD, MR
    [J]. EMBO JOURNAL, 1991, 10 (09) : 2653 - 2659
  • [6] MOLECULAR-CLONING, CHROMOSOMAL MAPPING, AND EXPRESSION OF THE CDNA FOR P107, A RETINOBLASTOMA GENE PRODUCT-RELATED PROTEIN
    EWEN, ME
    XING, YG
    LAWRENCE, JB
    LIVINGSTON, DM
    [J]. CELL, 1991, 66 (06) : 1155 - 1164
  • [7] CELL-CYCLE REGULATION OF HISTONE-H1 KINASE-ACTIVITY ASSOCIATED WITH THE ADENOVIRAL PROTEIN-E1A
    GIORDANO, A
    LEE, JH
    SCHEPPLER, JA
    HERRMANN, C
    HARLOW, E
    DEUSCHLE, U
    BEACH, D
    FRANZA, BR
    [J]. SCIENCE, 1991, 253 (5025) : 1271 - 1275
  • [8] ISOLATION OF THE RB-RELATED P130 THROUGH ITS INTERACTION WITH CDK2 AND CYCLINS
    HANNON, GJ
    DEMETRICK, D
    BEACH, D
    [J]. GENES & DEVELOPMENT, 1993, 7 (12A) : 2378 - 2391
  • [9] A CELL-CYCLE REGULATOR POTENTIALLY INVOLVED IN GENESIS OF MANY TUMOR TYPES
    KAMB, A
    GRUIS, NA
    WEAVERFELDHAUS, J
    LIU, QY
    HARSHMAN, K
    TAVTIGIAN, SV
    STOCKERT, E
    DAY, RS
    JOHNSON, BE
    SKOLNICK, MH
    [J]. SCIENCE, 1994, 264 (5157) : 436 - 440
  • [10] KIESS M, 1995, CELL GROWTH DIFFER, V6, P1287