STRUCTURE AND CHROMOSOME LOCALIZATION OF THE HUMAN EOSINOPHIL-DERIVED NEUROTOXIN AND EOSINOPHIL CATIONIC PROTEIN GENES - EVIDENCE FOR INTRONLESS CODING SEQUENCES IN THE RIBONUCLEASE GENE SUPERFAMILY

被引:96
作者
HAMANN, KJ
TEN, RM
LOEGERING, DA
JENKINS, RB
HEISE, MT
SCHAD, CR
PEASE, LR
GLEICH, GJ
BARKER, RL
机构
[1] MAYO CLIN & MAYO FDN, DEPT MED, ROCHESTER, MN 55905 USA
[2] MAYO CLIN & MAYO FDN, DEPT LAB MED, ROCHESTER, MN 55905 USA
关键词
D O I
10.1016/0888-7543(90)90197-3
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
Human genomic DNAs for the eosinophil granule proteins, eosinophil-derived neurotoxin (EDN) and eosinophil cationic protein (ECP), were isolated from genomic libraries. Alignment of EDN (RNS2) and ECP (RNS3) gene sequences demonstrated remarkable nucleotide similarities in noncoding sequences, introns, and flanking regions, as well as in the previously known coding regions. Detailed examination of the 5′-noncoding regions yielded putative TATA and CAAT boxes, as well as similarities to promoter motifs from unrelated genes. A single intron of 230 bases was found in the 5′ untranslated region and we suggest that a single intron in this region and an intronless coding region are features common to many members of the RNase gene superfamily. The RNS2 and RNS3 genes were localized to the q24-q31 region of human chromosome 14. It is likely that these two genes arose as a consequence of a gene duplication event that took place approximately 25-40 million years ago and that a subset of anthropoid primates possess both of these genes or closely related genes. © 1990.
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页码:535 / 546
页数:12
相关论文
共 62 条
[1]   COMPARATIVE TOXICITY OF PURIFIED HUMAN EOSINOPHIL GRANULE CATIONIC PROTEINS FOR SCHISTOSOMULA OF SCHISTOSOMA-MANSONI [J].
ACKERMAN, SJ ;
GLEICH, GJ ;
LOEGERING, DA ;
RICHARDSON, BA ;
BUTTERWORTH, AE .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1985, 34 (04) :735-745
[2]  
[Anonymous], 1987, MOL EVOLUTIONARY GEN, DOI DOI 10.7312/NEI-92038
[3]   ON THE VIRTUES AND PITFALLS OF THE MOLECULAR EVOLUTIONARY CLOCK [J].
AYALA, FJ .
JOURNAL OF HEREDITY, 1986, 77 (04) :226-235
[4]   A LYMPHOCYTE-SPECIFIC CELLULAR ENHANCER IS LOCATED DOWNSTREAM OF THE JOINING REGION IN IMMUNOGLOBULIN HEAVY-CHAIN GENES [J].
BANERJI, J ;
OLSON, L ;
SCHAFFNER, W .
CELL, 1983, 33 (03) :729-740
[5]   CLONING AND SEQUENCE-ANALYSIS OF THE HUMAN GENE ENCODING EOSINOPHIL MAJOR BASIC-PROTEIN [J].
BARKER, RL ;
LOEGERING, DA ;
ARAKAWA, KC ;
PEASE, LR ;
GLEICH, GJ .
GENE, 1990, 86 (02) :285-289
[6]  
BARKER RL, 1989, J IMMUNOL, V143, P952
[7]   AMINO-ACID SEQUENCE OF THE NONSECRETORY RIBONUCLEASE OF HUMAN-URINE [J].
BEINTEMA, JJ ;
HOFSTEENGE, J ;
IWAMA, M ;
MORITA, T ;
OHGI, K ;
IRIE, M ;
SUGIYAMA, RH ;
SCHIEVEN, GL ;
DEKKER, CA ;
GLITZ, DG .
BIOCHEMISTRY, 1988, 27 (12) :4530-4538
[8]  
BERCHTOLD MW, 1987, J BIOL CHEM, V262, P8696
[9]   ARRANGEMENT OF SIMIAN-VIRUS 40 SEQUENCES IN DNA OF TRANSFORMED-CELLS [J].
BOTCHAN, M ;
TOPP, W ;
SAMBROOK, J .
CELL, 1976, 9 (02) :269-287
[10]   OVALBUMIN GENE - EVIDENCE FOR A LEADER SEQUENCE IN MESSENGER-RNA AND DNA SEQUENCES AT EXON-INTRON BOUNDARIES [J].
BREATHNACH, R ;
BENOIST, C ;
OHARE, K ;
GANNON, F ;
CHAMBON, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (10) :4853-4857