EXPRESSION OF DNA-SEQUENCES CONTAINING NEURON SPECIFIC ENOLASE GENE IN ESCHERICHIA-COLI

被引:7
作者
DUTTA, SK
BHATTACHARYYA, N
PARUI, R
VERMA, M
机构
[1] HOWARD UNIV,DEPT BOT GENET & HUMAN GENET,WASHINGTON,DC 20059
[2] HOWARD UNIV,CANC RES CTR,WASHINGTON,DC 20059
[3] HOWARD UNIV HOSP,DEPT MED GENET,WASHINGTON,DC 20060
关键词
D O I
10.1016/S0006-291X(05)81046-0
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
There is evidence that the gene for gamma-gamma enolase (neuron specific enolase, NSE) is regulated during cell differentiation and development, conserved in a variety of organisms and contains mRNA destabilizing sequences. In order to investigate further the mechanisms of these processes and to obtain large quantity of this protein, the NSE gene was isolated from neuroblastoma cells and cloned in E. coli using standard molecular biology techniques. The NSE gene expression was studied and the expressed proptein (recombinant NSE) was characterized extensively. The recombinant NSE behaves like parental NSE in antisera specificity, resistance for chaotropic agents like urea, thermal stability at higher temperatures etc. The physical parameters like secondary structure, hydrophilicity, antigenic index and flexibility of the expressed protein were studied. The results of the present investigation collectively form the basis for initial investigations of how the expression of NSE gene is regulated. This is the first report where the recombinant NSE gene has been characterized so extensively. © 1990 Academic Press, Inc.
引用
收藏
页码:231 / 239
页数:9
相关论文
共 39 条
[1]   ORTHO-PHTHALALDEHYDE - FLUOROGENIC DETECTION OF PRIMARY AMINES IN PICOMOLE RANGE - COMPARISON WITH FLUORESCAMINE AND NINHYDRIN [J].
BENSON, JR ;
HARE, PE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1975, 72 (02) :619-622
[2]  
BIRLEY AJ, 1986, DNA SYSTEMATICS, V1, P107
[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]  
Chou P Y, 1978, Adv Enzymol Relat Areas Mol Biol, V47, P45
[5]   SEQUENCE CONSERVATION IN THE 3'-UNTRANSLATED REGIONS OF NEURON-SPECIFIC ENOLASE, LYMPHOKINE AND PROTOONCOGENE MESSENGER-RNAS [J].
DAY, INM ;
ALLSOPP, MTEP ;
MOORE, DCM ;
THOMPSON, RJ .
FEBS LETTERS, 1987, 222 (01) :139-143
[6]  
DUTTA SK, 1987, BIOCHEM INT, V15, P223
[7]  
DUTTA SK, 1987, NUCLEUS, V30, P77
[8]  
DUTTA SK, 1988, GENOME, V30, P177
[9]   INDUCTION OF HEPATITIS-A VIRUS-NEUTRALIZING ANTIBODY BY A VIRUS-SPECIFIC SYNTHETIC PEPTIDE [J].
EMINI, EA ;
HUGHES, JV ;
PERLOW, DS ;
BOGER, J .
JOURNAL OF VIROLOGY, 1985, 55 (03) :836-839
[10]   NEURON-SPECIFIC ENOLASE - COMPLETE STRUCTURE OF RAT MESSENGER-RNA, MULTIPLE TRANSCRIPTIONAL START SITES, AND EVIDENCE SUGGESTING POSTTRANSCRIPTIONAL CONTROL [J].
FORSSPETTER, S ;
DANIELSON, P ;
SUTCLIFFE, JG .
JOURNAL OF NEUROSCIENCE RESEARCH, 1986, 16 (01) :141-156