Cloning of ARE-containing genes by AU-motif-directed display

被引:10
作者
Dominguez, O
Ashhab, Y
Sabater, L
Belloso, E
Caro, P
Pujol-Borrell, R [1 ]
机构
[1] Autonomous Univ Barcelona, Univ Hosp Germans Trias Pujol, Immunol Unit, Badalona 08916, Spain
[2] Autonomous Univ Barcelona, Univ Hosp Germans Trias Pujol, Almirall Prodesfarma Res Ctr, Badalona 08916, Spain
关键词
D O I
10.1006/geno.1998.5548
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A procedure suitable for cloning labile mRNAs that contain AU motifs is presented (AU-DD). These motifs are regulatory sequences within the so-called AU-rich elements (AREs) often found in 3' untranslated regions of genes such as cytokines, proto-oncogenes, and transcription factors. AU-DD is an AU-motif-directed differential display that permits the identification of ARE-containing genes differentially expressed after cell activation. It has been applied to peripheral blood monocytes and a T cell clone to isolate 59 cDNA fragments associated to activation. Fourteen percent of isolated fragments belong to already known genes that certainly are cytokines and transduction/transcription factors. The remaining 86% correspond to unknown genes of which 92% have been confirmed to be differentially expressed. These data demonstrate the efficiency of the system and support the notion that numerous genes falling into those categories remain unidentified and that they can be cloned by this method. (C) 1998 Academic Press.
引用
收藏
页码:278 / 286
页数:9
相关论文
共 21 条
[1]  
ABRINK M, 1994, LEUKEMIA, V8, P1579
[2]  
ADAMS MD, 1995, NATURE, V377, P3
[3]   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
[4]   AU-RICH ELEMENTS - CHARACTERIZATION AND IMPORTANCE IN MESSENGER-RNA DEGRADATION [J].
CHEN, CYA ;
SHYU, AB .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (11) :465-470
[5]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[6]   IDENTIFICATION BY TARGETED DIFFERENTIAL DISPLAY OF AN IMMEDIATE-EARLY GENE ENCODING A PUTATIVE SERINE/THREONINE KINASE [J].
DONOHUE, PJ ;
ALBERTS, GF ;
GUO, Y ;
WINKLES, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (17) :10351-10357
[7]   PROTEIN-SYNTHESIS INHIBITORS DIFFERENTIALLY SUPERINDUCE C-FOS AND C-JUN BY 3 DISTINCT MECHANISMS - LACK OF EVIDENCE FOR LABILE REPRESSORS [J].
EDWARDS, DR ;
MAHADEVAN, LC .
EMBO JOURNAL, 1992, 11 (07) :2415-2424
[8]   RESTRICTION FRAGMENT LENGTH POLYMORPHISM-COUPLED DOMAIN-DIRECTED DIFFERENTIAL DISPLAY - A HIGHLY EFFICIENT TECHNIQUE FOR EXPRESSION ANALYSIS OF MULTIGENE FAMILIES [J].
FISCHER, A ;
SAEDLER, H ;
THEISSEN, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (12) :5331-5335
[9]   Identification of rapid turnover transcripts overexpressed in thyroid tumors and thyroid cancer cell lines: use of a targeted differential RNA display method to select for mRNA subsets [J].
Gonsky, R ;
Knauf, JA ;
Elisei, R ;
Wang, JW ;
Su, S ;
Fagin, JA .
NUCLEIC ACIDS RESEARCH, 1997, 25 (19) :3823-3831
[10]   Application of modified differential display technique for cloning and sequencing of the 3' region from three putative members of wheat HSP70 gene family [J].
Joshi, CP ;
Kumar, S ;
Nguyen, HT .
PLANT MOLECULAR BIOLOGY, 1996, 30 (03) :641-646