Beyond the cell cycle: A new role for cdk6 in differentiation

被引:71
作者
Grossel, MJ
Hinds, PW
机构
[1] Connecticut Coll, Dept Biol, New London, CT 06371 USA
[2] Tufts New England Med Ctr, Dept Radiat Oncol, Mol Oncol & Res Inst, Boston, MA USA
[3] Tufts Univ, New England Med Ctr, Dept Radiat Oncol, Mol Oncol & Res Inst, Boston, MA 02111 USA
关键词
cdk6; differentiation; G; phase; pRb; cdk4; cyclin D;
D O I
10.1002/jcb.20712
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
Over 10 years ago, cdk6 was identified as a new member in a family of vertebrate cdc-2 related kinases. This novel kinase was found to partner with the D-type cyclins and to possess pRb kinase activity in vitro and has since been understood to function solely as a pRb kinase in the regulation of the G, phase of the cell cycle. In the past 2 years, several independent Studies in multiple cell types have indicated a novel role for cdk6 in differentiation. For example, cdk6 expression must be reduced to allow proper osteoblast and osteoclast differentiation, forced cdk6 expression blocked differentiation of mouse erythroid leukemia cells and cdk6 expression in primary astrocytes favors the expression of progenitor cell markers. Since exit from the cell cycle is a necessary step in terminal differentiation, down-regulation of a mitogenic factor may be expected in this process, however it is Surprising that this association has not been previously uncovered and that it is apparently not shared with cdk4, long understood to be a functional homolog of cdk6. The mechanism of cdk6 function in differentiation is not understood, but it may extend beyond the established role of cdk6 as a pRb kinase. As this story unfolds it will be important to discover if the function of cdk6 in differentiation is pRb-dependent or pRb-independent, since pRb has long been established as a key factor in initiating and maintaining cell cycle exit during differentiation.
引用
收藏
页码:485 / 493
页数:9
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  • [21] Lucas JJ, 2004, MOL CANCER RES, V2, P105
  • [22] DIFFERENTIAL REGULATION OF THE SYNTHESIS AND ACTIVITY OF THE MAJOR CYCLIN-DEPENDENT KINASES, P34(CDC2), P33(CDK2), AND P34(CDK4), DURING CELL-CYCLE ENTRY AND PROGRESSION IN NORMAL HUMAN T-LYMPHOCYTES
    LUCAS, JJ
    SZEPESI, A
    DOMENICO, J
    TORDAI, A
    TERADA, N
    GELFAND, EW
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 1995, 165 (02) : 406 - 416
  • [23] Active cdk6 complexes are predominantly nuclear and represent only a minority of the cdk6 in T cells
    Mahony, D
    Parry, DA
    Lees, E
    [J]. ONCOGENE, 1998, 16 (05) : 603 - 611
  • [24] Mammalian cells cycle without the D-type cyclin-elependent kinases Cdk4 and Cdk6
    Malumbres, M
    Sotillo, R
    Santamaria, D
    Galán, J
    Cerezo, A
    Ortega, S
    Dubus, P
    Barbacid, M
    [J]. CELL, 2004, 118 (04) : 493 - 504
  • [25] CELL BIOLOGY - CELL-CYCLE INHIBITORS MAY HELP BRAKE GROWTH AS CELLS DEVELOP
    MARX, J
    [J]. SCIENCE, 1995, 267 (5200) : 963 - 964
  • [26] IDENTIFICATION AND PROPERTIES OF AN ATYPICAL CATALYTIC SUBUNIT (P34(PSK-J3)/CDK4) FOR MAMMALIAN-D TYPE-G1 CYCLINS
    MATSUSHIME, H
    EWEN, ME
    STROM, DK
    KATO, JY
    HANKS, SK
    ROUSSEL, MF
    SHERR, CJ
    [J]. CELL, 1992, 71 (02) : 323 - 334
  • [27] D-TYPE CYCLIN-DEPENDENT KINASE-ACTIVITY IN MAMMALIAN-CELLS
    MATSUSHIME, H
    QUELLE, DE
    SHURTLEFF, SA
    SHIBUYA, M
    SHERR, CJ
    KATO, JY
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (03) : 2066 - 2076
  • [28] Cyclin-dependent kinases regulate the antiproliferative function of Smads
    Matsuura, I
    Denissova, NG
    Wang, GN
    He, DM
    Long, JY
    Liu, F
    [J]. NATURE, 2004, 430 (6996) : 226 - 231
  • [29] CDK6 blocks differentiation: coupling cell proliferation to the block to differentiation in leukemic cells
    Matushansky, I
    Radparvar, F
    Skoultchi, AI
    [J]. ONCOGENE, 2003, 22 (27) : 4143 - 4149
  • [30] Reprogramming leukemic cells to terminal differentiation by inhibiting specific cyclin-dependent kinases in G1
    Matushansky, I
    Radparvar, F
    Skoultchi, AI
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (26) : 14317 - 14322