THE INTRACELLULAR-DISTRIBUTION AND PATTERN OF EXPRESSION OF MCL-1 OVERLAP WITH, BUT ARE NOT IDENTICAL TO, THOSE OF BCL-2

被引:263
作者
YANG, T
KOZOPAS, KM
CRAIG, RW
机构
[1] DARTMOUTH COLL, SCH MED, DEPT PHARMACOL & TOXICOL, HANOVER, NH 03755 USA
[2] JOHNS HOPKINS UNIV, SCH MED, DEPT PHYSIOL, BALTIMORE, MD 21205 USA
关键词
D O I
10.1083/jcb.128.6.1173
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A family of genes related to the bcl-2 protooncogene has recently emerged. One member of this family, mel-1, was cloned from a human myeloblastic leukemia cell line (ML-1) undergoing differentiation. The intracellular localization of mel-1, as well as the kinetics of its expression during differentiation, have now been studied. These studies show that the intracellular distribution of mel-1 overlaps with, but is not identical to, that of bcl-2: mel-1 is similar to bcl-2 in that the mel-1 protein has a prominent mitochondrial localization, and in that it associates with membranes through its carboxyl hydrophobic tail. mcl-1 differs from bcl-2, however, in its relative distribution among other (nonmitochondrial/heavy membrane) compartments, mel-1 also being abundant in the light membrane fraction of immature ML-I cells while bcl-2 is abundant in the nuclear fraction. Similarly, in differentiating ML-1 cells, the timing of expression of mel-1 overlaps with, but is not identical to, that of bcl-2: the mel-1 protein increases rapidly as cells initiate differentiation, and mel-1 is a labile protein. In contrast, bcl-2 decreases gradually as cells complete differentiation. Overall, the mel-1 and bcl-2 proteins have some properties in common and others that are distinct. A burst of expression of mel-1, prominently associated with mitochondria, complements the continued expression of bcl-2 in ML-1 cells differentiating along the monocyte/macrophage pathway.
引用
收藏
页码:1173 / 1184
页数:12
相关论文
共 56 条
  • [1] AZORSA DO, 1991, BLOOD, V78, P280
  • [2] BANTIA S, 1990, BLOOD, V75, P1659
  • [3] APOPTOTIC CELL-DEATH INDUCED BY C-MYC IS INHIBITED BY BCL-2
    BISSONNETTE, RP
    ECHEVERRI, F
    MAHBOUBI, A
    GREEN, DR
    [J]. NATURE, 1992, 359 (6395) : 552 - 554
  • [4] BCL-X, A BCL-2-RELATED GENE THAT FUNCTIONS AS A DOMINANT REGULATOR OF APOPTOTIC CELL-DEATH
    BOISE, LH
    GONZALEZGARCIA, M
    POSTEMA, CE
    DING, LY
    LINDSTEN, T
    TURKA, LA
    MAO, XH
    NUNEZ, G
    THOMPSON, CB
    [J]. CELL, 1993, 74 (04) : 597 - 608
  • [5] BORDIER C, 1981, J BIOL CHEM, V256, P1604
  • [6] THE PROTEIN BCL-2-ALPHA DOES NOT REQUIRE MEMBRANE ATTACHMENT, BUT 2 CONSERVED DOMAINS TO SUPPRESS APOPTOSIS
    BORNER, C
    MARTINOU, I
    MATTMANN, C
    IRMLER, M
    SCHAERER, E
    MARTINOU, JC
    TSCHOPP, J
    [J]. JOURNAL OF CELL BIOLOGY, 1994, 126 (04) : 1059 - 1068
  • [7] CLONING AND STRUCTURAL-ANALYSIS OF CDNAS FOR BCL-2 AND A HYBRID BCL-2/IMMUNOGLOBULIN TRANSCRIPT RESULTING FROM THE T(14-18) TRANSLOCATION
    CLEARY, ML
    SMITH, SD
    SKLAR, J
    [J]. CELL, 1986, 47 (01) : 19 - 28
  • [8] CRAIG RW, 1993, CELL GROWTH DIFFER, V4, P349
  • [9] CRAIG RW, 1984, CANCER RES, V44, P2421
  • [10] DIFFERENTIATION-INDUCING AND CYTO-TOXIC EFFECTS OF TUMOR NECROSIS FACTOR AND INTERFERON-GAMMA IN MYELOBLASTIC ML-1 CELLS
    CRAIG, RW
    BUCHAN, HL
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 1989, 141 (01) : 46 - 52