CHARACTERIZATION OF THE MOUSE BETA-MAJ GLOBIN TRANSCRIPTION TERMINATION REGION - A SPACING SEQUENCE IS REQUIRED BETWEEN THE POLY(A) SIGNAL SEQUENCE AND MULTIPLE DOWNSTREAM TERMINATION ELEMENTS

被引:48
作者
TANTRAVAHI, J [1 ]
ALVIRA, M [1 ]
FALCKPEDERSEN, E [1 ]
机构
[1] CORNELL UNIV,MED CTR,COLL MED,W RANDOLPH HEARST FDN,DEPT MICROBIOL,1300 YORK AVE,NEW YORK,NY 10021
关键词
D O I
10.1128/MCB.13.1.578
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
For the majority of mRNA encoding eukaryotic transcription units, there is little or no knowledge of the elements responsible for transcription termination or how they may interact with RNA polymerase. In this report, we have used recombinant adenovirus reporter vectors to characterize the mouse beta(maj) globin sequence elements that cause transcription termination. Within the globin 3' termination region, we have identified at least three sequence elements which induce significant levels of transcription termination (> 50%). The smallest functionally active element (64% termination) is 69 bp in length. The natural arrangement of these elements results in a cumulative termination which is greater than 90%. Recognition of the termination elements by RNA polymerase II depends on the presence of a functional poly(A) signal sequence. We demonstrate that efficient transcription termination depends on appropriate spacing between the poly(A) signal sequence and the termination element.
引用
收藏
页码:578 / 587
页数:10
相关论文
共 46 条
[1]   3' EDITING OF MESSENGER-RNAS - SEQUENCE REQUIREMENTS AND INVOLVEMENT OF A 60-NUCLEOTIDE RNA IN MATURATION OF HISTONE MESSENGER-RNA PRECURSORS [J].
BIRCHMEIER, C ;
SCHUMPERLI, D ;
SCONZO, G ;
BIRNSTIEL, ML .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (04) :1057-1061
[2]   TRANSCRIPTION TERMINATION AND 3' PROCESSING - THE END IS IN SITE [J].
BIRNSTIEL, ML ;
BUSSLINGER, M ;
STRUB, K .
CELL, 1985, 41 (02) :349-359
[3]   AN INTACT HISTONE 3'-PROCESSING SITE IS REQUIRED FOR TRANSCRIPTION TERMINATION IN A MOUSE HISTONE H2A GENE [J].
CHODCHOY, N ;
PANDEY, NB ;
MARZLUFF, WF .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (01) :497-509
[4]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[5]   FORMATION OF THE 3' END ON U SNRNAS REQUIRES AT LEAST 3 SEQUENCE ELEMENTS [J].
CILIBERTO, G ;
DATHAN, N ;
FRANK, R ;
PHILIPSON, L ;
MATTAJ, IW .
EMBO JOURNAL, 1986, 5 (11) :2931-2937
[6]   TRANSCRIPTION TERMINATION OCCURS WITHIN A 1000 BASE PAIR REGION DOWNSTREAM FROM THE POLY(A) SITE OF THE MOUSE BETA-GLOBIN (MAJOR) GENE) [J].
CITRON, B ;
FALCKPEDERSEN, E ;
SALDITTGEORGIEFF, M ;
DARNELL, JE .
NUCLEIC ACIDS RESEARCH, 1984, 12 (22) :8723-8731
[7]   A CCAAT BOX SEQUENCE IN THE ADENOVIRUS MAJOR LATE PROMOTER FUNCTIONS AS PART OF AN RNA POLYMERASE-II TERMINATION SIGNAL [J].
CONNELLY, S ;
MANLEY, JL .
CELL, 1989, 57 (04) :561-571
[8]   A FUNCTIONAL MESSENGER-RNA POLYADENYLATION SIGNAL IS REQUIRED FOR TRANSCRIPTION TERMINATION BY RNA POLYMERASE-II [J].
CONNELLY, S ;
MANLEY, JL .
GENES & DEVELOPMENT, 1988, 2 (04) :440-452
[9]   RNA POLYMERASE-II TRANSCRIPTION TERMINATION IS MEDIATED SPECIFICALLY BY PROTEIN-BINDING TO A CCAAT BOX SEQUENCE [J].
CONNELLY, S ;
MANLEY, JL .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (11) :5254-5259
[10]   CYCLOHEXIMIDE STIMULATES EARLY ADENOVIRUS TRANSCRIPTION IF EARLY GENE-EXPRESSION IS ALLOWED BEFORE TREATMENT [J].
CROSS, FR ;
DARNELL, JE .
JOURNAL OF VIROLOGY, 1983, 45 (02) :683-692