IMPROVED ACCUMULATION AND ACTIVITY OF RIBOZYMES EXPRESSED FROM A TRANSFER-RNA-BASED RNA-POLYMERASE-III PROMOTER

被引:73
作者
THOMPSON, JD
AYERS, DF
MALMSTROM, TA
MCKENZIE, TL
GANOUSIS, L
CHOWRIRA, BM
COUTURE, L
STINCHCOMB, DT
机构
[1] Ribozyme Pharmaceuticals Inc., Boulder, CO 80301
关键词
D O I
10.1093/nar/23.12.2259
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
RNA polymerase III (pol III) transcripts am abundant in all cells. Therefore, pol III promoters may be ideal for expressing high levels of exogenous RNAs, such as antisense RNAs, decoy RNAs and ribozymes, in many different cell types. We have improved accumulation of recombinant RNAs expressed from a human met(i) tRNA-derived pol III promoter >100-fold by modifying the 3' terminus of the transcripts to hybridize to the 5' terminus. This terminal duplex includes the 8 nt leader sequence present in the primary wild-type met(i) tRNA transcript that is normally removed during processing to the mature tRNA. Expression of an anti-HIV ribozyme was analyzed in cells stably transduced with retroviral vectors encoding pol III transcription units containing this modification. High accumulation of recombinant pol III ribozyme transcripts was observed in all cell lines tested. Due to the enhanced transcript accumulation, ribozyme cleavage activity was readily detectable in total RNA extracted from stably transduced human T cell lines. One pol III transcription unit, termed 'TRZ', was optimized further for ribozyme cleavage activity. The improved pol III transcription units reported here may be useful for expressing a variety of functional and therapeutic RNAs.
引用
收藏
页码:2259 / 2268
页数:10
相关论文
共 35 条
[1]   GENERATION OF LONG READ-THROUGH TRANSCRIPTS INVIVO AND INVITRO BY DELETION OF 3' TERMINATION AND PROCESSING SEQUENCES IN THE HUMAN TRANSFER RNAIMET GENE [J].
ADENIYIJONES, S ;
ROMEO, PH ;
ZASLOFF, M .
NUCLEIC ACIDS RESEARCH, 1984, 12 (02) :1101-1115
[2]  
BALTIMORE D, 1988, NATURE, V325, P395
[3]   CAN HAMMERHEAD RIBOZYMES BE EFFICIENT TOOLS TO INACTIVATE GENE-FUNCTION [J].
BERTRAND, E ;
PICTET, R ;
GRANGE, T .
NUCLEIC ACIDS RESEARCH, 1994, 22 (03) :293-300
[4]   CONSTITUTIVE EXPRESSION OF CHIMERIC NEO-REV RESPONSE ELEMENT TRANSCRIPTS SUPPRESSES HIV-1 REPLICATION IN HUMAN CD4(+) T-LYMPHOCYTES [J].
BEVEC, D ;
VOLCPLATZER, B ;
ZIMMERMANN, K ;
DOBROVNIK, M ;
HAUBER, J ;
VERES, G ;
BOHNLEIN, E .
HUMAN GENE THERAPY, 1994, 5 (02) :193-201
[5]   SELECTION OF SINGLE-STRANDED-DNA MOLECULES THAT BIND AND INHIBIT HUMAN THROMBIN [J].
BOCK, LC ;
GRIFFIN, LC ;
LATHAM, JA ;
VERMAAS, EH ;
TOOLE, JJ .
NATURE, 1992, 355 (6360) :564-566
[6]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[7]   GENE-THERAPY FOR HUMAN-IMMUNODEFICIENCY-VIRUS INFECTION - GENETIC ANTIVIRAL STRATEGIES AND TARGETS FOR INTERVENTION [J].
DROPULIC, B ;
JEANG, KT .
HUMAN GENE THERAPY, 1994, 5 (08) :927-939
[8]  
DROPULIC B, 1991, J VIROL, V66, P1432
[9]  
FORSTER AC, 1987, CELL, V80, P9
[10]   TRANSCRIPTION BY RNA POLYMERASE-III [J].
GEIDUSCHEK, EP ;
TOCCHINIVALENTINI, GP .
ANNUAL REVIEW OF BIOCHEMISTRY, 1988, 57 :873-914