IRRADIATION INCREASES LEVELS OF GM-CSF THROUGH RNA STABILIZATION WHICH REQUIRES AN AU-RICH REGION IN CANCER-CELLS

被引:29
作者
AKASHI, M
HACHIYA, M
KOEFFLER, HP
SUZUKI, G
机构
[1] UNIV CALIF LOS ANGELES,CTR HLTH SCI,SCH MED,DIV HEMATOL ONCOL,LOS ANGELES,CA 90024
[2] UNIV CALIF LOS ANGELES,CEDARS SINAI MED CTR,SCH MED,DIV HEMATOL ONCOL,LOS ANGELES,CA 90048
关键词
D O I
10.1016/0006-291X(92)92301-D
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
Granulocyte/macrophage colony stimulating factor (GM-CSF) is a hematopoietic growth factor that stimulates a wide range of myeloid hematopoietic cells; RNAs coding for many oncogenes and cytokines including GM-CSF have a very short half-life. The motif of AUUA is a highly conserved sequence in the 3'untranslated regions (3'UTR) of these transcripts and is repeated a number of times in these short-lived cytokines and oncogenes. These sequences play a major role in controlling stability of these transcripts. Human cancer cells were transfected with a chimeric rabbit β-globin gene linked to either a 58 bp sequence of the AT-rich region from GM-CSF or a control sequence. We have found that irradiation stimulates accumulation of GM-CSF, interleukin-6 (IL-6), and IL-1 β RNAs. In addition, this accumulation of GM-CSF was at least, in part, a result of increased stabilization of GM-CSF transcripts. Further experiments showed that irradiation increased levels of the chimeric β-globin transcripts containing AUUUA sequences from GM-CSF, but not those containing the control sequences. Our results suggest that irradiation increases expression of GM-CSF RNA and that posttranscriptional stabilization requiring AUUUA sequences probably is in part one of the mechanisms producing the increased levels of GM-CSF RNA by irradiation. © 1992.
引用
收藏
页码:986 / 993
页数:8
相关论文
共 29 条
[1]  
AKASHI M, 1991, BLOOD, V78, P2005
[2]  
AKASHI M, 1989, BLOOD, V74, P383
[3]   AN INDUCIBLE CYTOPLASMIC FACTOR (AU-B) BINDS SELECTIVELY TO AUUUA MULTIMERS IN THE 3' UNTRANSLATED REGION OF LYMPHOKINE MESSENGER-RNA [J].
BOHJANEN, PR ;
PETRYNIAK, B ;
JUNE, CH ;
THOMPSON, CB ;
LINDSTEN, T .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (06) :3288-3295
[4]   IONIZING-RADIATION INDUCES EXPRESSION AND BINDING-ACTIVITY OF THE NUCLEAR FACTOR-KAPPA-B [J].
BRACH, MA ;
HASS, R ;
SHERMAN, ML ;
GUNJI, H ;
WEICHSELBAUM, R ;
KUFE, D .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (02) :691-695
[5]   IDENTIFICATION OF A COMMON NUCLEOTIDE-SEQUENCE IN THE 3'-UNTRANSLATED REGION OF MESSENGER-RNA MOLECULES SPECIFYING INFLAMMATORY MEDIATORS [J].
CAPUT, D ;
BEUTLER, B ;
HARTOG, K ;
THAYER, R ;
BROWNSHIMER, S ;
CERAMI, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (06) :1670-1674
[6]  
CEBON J, 1988, BLOOD, V72, P1340
[7]   TRANSCRIPTIONAL ENHANCERS FROM SV40 AND POLYOMA-VIRUS SHOW A CELL TYPE PREFERENCE [J].
DEVILLIERS, J ;
OLSON, L ;
TYNDALL, C ;
SCHAFFNER, W .
NUCLEIC ACIDS RESEARCH, 1982, 10 (24) :7965-7976
[8]  
DIPERSIO JF, 1978, BLOOD, V51, P507
[9]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[10]   MOLECULAR PHYSIOLOGY OF GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR [J].
GASSON, JC .
BLOOD, 1991, 77 (06) :1131-1145