Structural characterization and mapping of the normal epithelial cell-specific 1 gene

被引:55
作者
Luo, LY
Herbrick, JA
Scherer, SW
Beatty, B
Squire, J
Diamandis, EP
机构
[1] Mt Sinai Hosp, Dept Pathol & Lab Med, Toronto, ON M5G 1X5, Canada
[2] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[3] Hosp Sick Children, Dept Genet, Toronto, ON M5G 1X8, Canada
[4] Univ Toronto, Dept Mol & Med Genet, Toronto, ON, Canada
[5] Princess Margaret Hosp, Ontario Canc Inst, Toronto, ON M4X 1K9, Canada
基金
英国医学研究理事会;
关键词
breast cancer; gene mapping; kallikrein genes; NES1; gene; NES1 genomic structure;
D O I
10.1006/bbrc.1998.8793
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 normal epithelial cell-specific 1 (NES1) gene is a recently identified novel serine protease-like gene which is down-regulated during breast cancer progression. The gene product has 34-42% identity with the members of three distinct serine protease families: the trypsin-like family, activators of kringle domain-containing growth factors, and the kallikrein family (X. L. Liu et al., (1996) Cancer Res 56, 3371-3379), Although the cDNA of this gene has been cloned, its genomic structure and chromosomal position are not as yet known, Here, we report the genomic characterization and mapping of the NES1 gene. By subcloning and sequencing a PAC clone containing the complete NES1 gene, we were able to characterize the structure of this gene. The NES1 gene spans 5.5 kb and is composed of five coding exons and one untranslated exon, The positions of the introns were similar to trypsinogen, prostate specific antigen (PSA), and tissue plasminogen activator (TPA). NES1 gene was also localized with somatic cell mapping, radiation hybrid mapping, and fluorescence in situ hybridization techniques to chromosome 19q13.3-q13.4, the same region where the human kallikrein gene family resides. Taken together, our results suggest that the NES1 gene originates from the same ancestor as trpsinogen, PSA, and TPA, but remains in close proximity to PSA. (C) 1998 Academic Press.
引用
收藏
页码:580 / 586
页数:7
相关论文
共 30 条
[1]   A novel protease homolog differentially expressed in breast and ovarian cancer [J].
Anisowicz, A ;
Sotiropoulou, G ;
Stenman, G ;
Mok, SC ;
Sager, R .
MOLECULAR MEDICINE, 1996, 2 (05) :624-636
[2]   REFINED 2 A X-RAY CRYSTAL-STRUCTURE OF PORCINE PANCREATIC KALLIKREIN-A, A SPECIFIC TRYPSIN-LIKE SERINE PROTEINASE - CRYSTALLIZATION, STRUCTURE DETERMINATION, CRYSTALLOGRAPHIC REFINEMENT, STRUCTURE AND ITS COMPARISON WITH BOVINE TRYPSIN [J].
BODE, W ;
CHEN, ZG ;
BARTELS, K ;
KUTZBACH, C ;
SCHMIDTKASTNER, G ;
BARTUNIK, H .
JOURNAL OF MOLECULAR BIOLOGY, 1983, 164 (02) :237-282
[3]   WEIGHT MATRIX DESCRIPTIONS OF 4 EUKARYOTIC RNA POLYMERASE-II PROMOTER ELEMENTS DERIVED FROM 502 UNRELATED PROMOTER SEQUENCES [J].
BUCHER, P .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 212 (04) :563-578
[4]  
COLLEN D, 1980, THROMB HAEMOSTASIS, V43, P77
[5]   TERTIARY STRUCTURAL DIFFERENCES BETWEEN MICROBIAL SERINE PROTEASES AND PANCREATIC SERINE ENZYMES [J].
DELBAERE, LTJ ;
HUTCHEON, WLB ;
JAMES, MNG ;
THIESSEN, WE .
NATURE, 1975, 257 (5529) :758-763
[6]   NEW BIOLOGICAL FUNCTIONS OF PROSTATE-SPECIFIC ANTIGEN [J].
DIAMANDIS, EP ;
YU, H .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1995, 80 (05) :1515-1517
[7]   NUCLEOTIDE-SEQUENCE AND ORGANIZATION OF THE MOUSE ADENINE PHOSPHORIBOSYLTRANSFERASE GENE - PRESENCE OF A CODING REGION COMMON TO ANIMAL AND BACTERIAL PHOSPHORIBOSYLTRANSFERASES THAT HAS A VARIABLE INTRON EXON ARRANGEMENT [J].
DUSH, MK ;
SIKELA, JM ;
KHAN, SA ;
TISCHFIELD, JA ;
STAMBROOK, PJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (09) :2731-2735
[8]  
EMI M, 1986, GENE, V41, P305
[9]   STRUCTURE AND CHROMOSOMAL LOCALIZATION OF THE HUMAN RENAL KALLIKREIN GENE [J].
EVANS, BA ;
YUN, ZX ;
CLOSE, JA ;
TREGEAR, GW ;
KITAMURA, N ;
NAKANISHI, S ;
CALLEN, DF ;
BAKER, E ;
HYLAND, VJ ;
SUTHERLAND, GR ;
RICHARDS, RI .
BIOCHEMISTRY, 1988, 27 (09) :3124-3129
[10]   DIGITIZED AND DIFFERENTIALLY SHADED HUMAN-CHROMOSOME IDEOGRAMS FOR GENOMIC APPLICATIONS [J].
FRANCKE, U .
CYTOGENETICS AND CELL GENETICS, 1994, 65 (03) :206-218