THE CONTRIBUTION OF AAUAAA AND THE UPSTREAM ELEMENT UUUGUA TO THE EFFICIENCY OF MESSENGER-RNA 3'-END FORMATION IN PLANTS

被引:86
作者
ROTHNIE, HM
REID, J
HOHN, T
机构
[1] Friedrich Miescher Institute, CH4002 Basel
关键词
3'-END FORMATION; AAUAAA; CAULIFLOWER MOSAIC VIRUS; PARARETROVIRUS; PLANT MESSENGER-RNA; POLYADENYLATION; UPSTREAM ELEMENTS;
D O I
10.1002/j.1460-2075.1994.tb06497.x
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
The requirement for sequence specificity in the AAUAAA motif of the cauliflower mosaic virus (CaMV) polyadenylation signal was examined by saturation mutagenesis. While deletion of AAUAAA almost abolished processing at the CaMV polyadenylation site, none of the 18 possible single base mutations had a dramatic effect on processing efficiency. The effect of replacing all six nucleotides simultaneously varied depending on the sequence used, but some replacements were as detrimental as the deletion mutant. Taken together, these results confirm that AAUAAA is an essential component of the CaMV polyadenylation signal, but indicate that a high degree of sequence variation can be tolerated. A repeated UUUGUA moth was identified as an important upstream accessory element of the CaMV polyadenylation signal. This sequence was able to induce processing at a heterologous polyadenylation site in a sequence-specific and additive manner. The effect of altering the spacing between this upstream element and the AAUAAA was examined; moving these two elements closer together or further apart reduces the processing efficiency. The upstream element does not function to signal processing at the CaMV polyadenylation site if placed downstream of the cleavage site. Analysis of further upstream sequences revealed that almost all of the 200 nt fragment required for maximal processing contributes positively to processing efficiency. Furthermore, isolated far upstream sequences distinct from UUUGUA were also able to induce processing at a heterologous polyadenylation site.
引用
收藏
页码:2200 / 2210
页数:11
相关论文
共 63 条
[1]   SIGNAL SEQUENCE FOR GENERATION OF MESSENGER-RNA 3' END IN THE SACCHAROMYCES-CEREVISIAE GAL7 GENE [J].
ABE, A ;
HIRAOKA, Y ;
FUKASAWA, T .
EMBO JOURNAL, 1990, 9 (11) :3691-3697
[2]   SITE-DIRECTED RIBOSE METHYLATION IDENTIFIES 2'-OH GROUPS IN POLYADENYLATION SUBSTRATES CRITICAL FOR AAUAAA RECOGNITION AND POLY(A) ADDITION [J].
BARDWELL, VJ ;
WICKENS, M ;
BIENROTH, S ;
KELLER, W ;
SPROAT, BS ;
LAMOND, AI .
CELL, 1991, 65 (01) :125-133
[3]   STRUCTURE AND TRANSCRIPTION OF THE NOPALINE SYNTHASE GENE REGION OF T-DNA [J].
BEVAN, M ;
BARNES, WM ;
CHILTON, MD .
NUCLEIC ACIDS RESEARCH, 1983, 11 (02) :369-385
[4]  
BIENROTH S, 1991, J BIOL CHEM, V266, P19768
[5]   RNA PROCESSING GENERATES THE MATURE 3' END OF YEAST CYC1 MESSENGER-RNA INVITRO [J].
BUTLER, JS ;
PLATT, T .
SCIENCE, 1988, 242 (4883) :1270-1274
[6]   RNA PROCESSING INVITRO PRODUCES MATURE 3' ENDS OF A VARIETY OF SACCHAROMYCES-CEREVISIAE MESSENGER-RNAS [J].
BUTLER, JS ;
SADHALE, PP ;
PLATT, T .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (06) :2599-2605
[7]   EFFICIENCY OF UTILIZATION OF THE SIMIAN VIRUS-40 LATE POLYADENYLATION SITE - EFFECTS OF UPSTREAM SEQUENCES [J].
CARSWELL, S ;
ALWINE, JC .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (10) :4248-4258
[8]   SEPARATION OF FACTORS REQUIRED FOR CLEAVAGE AND POLYADENYLATION OF YEAST PRE-MESSENGER-RNA [J].
CHEN, J ;
MOORE, C .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (08) :3470-3481
[9]   3' CLEAVAGE AND POLYADENYLATION OF MESSENGER-RNA PRECURSORS INVITRO REQUIRES A POLY(A) POLYMERASE, A CLEAVAGE FACTOR, AND A SNRNP [J].
CHRISTOFORI, G ;
KELLER, W .
CELL, 1988, 54 (06) :875-889
[10]   MESSENGER-RNA TRANSCRIPTS OF SEVERAL PLANT GENES ARE POLYADENYLATED AT MULTIPLE SITES INVIVO [J].
DEAN, C ;
TAMAKI, S ;
DUNSMUIR, P ;
FAVREAU, M ;
KATAYAMA, C ;
DOONER, H ;
BEDBROOK, J .
NUCLEIC ACIDS RESEARCH, 1986, 14 (05) :2229-2240