TESTIS-SPECIFIC TRANSCRIPTION INITIATION SITES OF RAT FARNESYL PYROPHOSPHATE SYNTHETASE MESSENGER-RNA

被引:59
作者
TERUYA, JH
KUTSUNAI, SY
SPEAR, DH
EDWARDS, PA
CLARKE, CF
机构
[1] UNIV CALIF LOS ANGELES,SCH MED,DIV CARDIOL,10833 LE CONTE AVE,LOS ANGELES,CA 90024
[2] UNIV CALIF LOS ANGELES,SCH MED,DEPT BIOL CHEM,LOS ANGELES,CA 90024
关键词
D O I
10.1128/MCB.10.5.2315
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
A variety of rat tissues were screened at low stringency with a rat farnesyl pyrophosphate (FPP) synthetase cDNA. In testis, an FPP synthetase-related RNA was detected that was larger than the liver FPP synthetase mRNA and was present at very high levels comparable with liver FPP synthetase RNA levels obtained from rats fed diets supplemented with cholestyramine and mevinolin. Sequence analysis of testis cDNA clones, together with primer extension and S1 nuclease experiments, indicated that testis FPP synthetase transcripts contain an extended 5' untranslated region. The 5' extension contained one or two out-of-frame upstream ATGs, depending on the site of transcription initiation. Protein in vitro translation studies indicated that the extended 5' untranslated region may play a role in regulating the translation of the FPP synthetase polypeptide in rat testis. Southern blot anlaysis with a probe containing both testis and liver 5' untranslated sequences provided evidence that both liver and testis transcripts derive from the same gene. The data suggest that an upstream testis-specific promoter results in the abundant production of FPP synthetase transcripts that are translated at low efficiency; another promoter functions in liver and other somatic tissues and directs the regulated synthesis of shorter discrete transcripts.
引用
收藏
页码:2315 / 2326
页数:12
相关论文
共 55 条
[1]  
ASHBY MN, 1989, J BIOL CHEM, V264, P635
[2]  
BAKER HJ, 1979, LABORATORY RAT BIOL, V1, P1
[3]   REGULATION OF RAT-LIVER PHOSPHOENOLPYRUVATE CARBOXYKINASE (GTP) MESSENGER RIBONUCLEIC-ACID ACTIVITY BY N6,O2'-DIBUTYRYLADENOSINE 3',5'-PHOSPHATE [J].
BEALE, EG ;
KATZEN, CS ;
GRANNER, DK .
BIOCHEMISTRY, 1981, 20 (17) :4878-4883
[4]   INCORPORATION OF A PRODUCT OF MEVALONIC ACID METABOLISM INTO PROTEINS OF CHINESE-HAMSTER OVARY CELL-NUCLEI [J].
BECK, LA ;
HOSICK, TJ ;
SINENSKY, M .
JOURNAL OF CELL BIOLOGY, 1988, 107 (04) :1307-1316
[5]   ALTERNATIVE SPLICING - A UBIQUITOUS MECHANISM FOR THE GENERATION OF MULTIPLE PROTEIN ISOFORMS FROM SINGLE GENES [J].
BREITBART, RE ;
ANDREADIS, A ;
NADALGINARD, B .
ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 :467-495
[6]  
BROWN MS, 1980, J LIPID RES, V21, P505
[7]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[8]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[9]   ALTERNATIVE TRANSCRIPTION AND SPLICING OF THE HUMAN PORPHOBILINOGEN DEAMINASE GENE RESULT EITHER IN TISSUE-SPECIFIC OR IN HOUSEKEEPING EXPRESSION [J].
CHRETIEN, S ;
DUBART, A ;
BEAUPAIN, D ;
RAICH, N ;
GRANDCHAMP, B ;
ROSA, J ;
GOOSSENS, M ;
ROMEO, PH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (01) :6-10
[10]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995