Genomic structure and expression profile of LPHH1, a 7TM gene variably expressed in breast cancer cell lines

被引:9
作者
White, GRM
Varley, JM
Heighway, J
机构
[1] Roy Castle Int Ctr Lung Canc Res, Gene Funct Grp, Liverpool L3 9TA, Merseyside, England
[2] Christie Hosp NHS Trust, Paterson Inst Canc Res, CRC, Mol Genet Sect, Manchester M20 9BX, Lancs, England
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 2000年 / 1491卷 / 1-3期
关键词
breast cancer; alternative splicing; 7TM; latrophilin;
D O I
10.1016/S0167-4781(00)00020-8
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
Gene identification studies, centred on a region of overlapping loss of heterozygosity in breast tumours within band 1p31.1, lead to the characterisation of LPHH1, a novel human 7TM gene. The coding sequence of LPHH1 extends over a 60 kb region and comprises in excess of 28 exons. Alternative splicing occurs minimally at five positions, four of which are within the coding sequence. The fifth region of alternative splicing occurs at the extreme 5' end of the transcript. A clear tissue specific bias in alternative exon selection is observed to some degree at all five positions, including the extreme 5' region, which raises the possibility of multiple and perhaps tissue specific promoters. One such putative promoter region, which appears to be utilised predominantly in breast cancer cells, has been identified. LPHH1 is highly evolutionarily conserved, with the simplest (19 exon) gene product being 95% identical between human and rat. Comparison of the alternatively spliced exons between three species, where data are available, has so far revealed 100% identity in the encoded peptide sequences, suggesting conservation of a functional aspect of this splicing. Gene expression has been observed in all tissues and cell lines tested, with the exception of lymphoblastoid and multiple myeloma lines, where there appears to be only a very low level of transcription. LPHH1 also appears to be downregulated in human bone marrow. These data are consistent with a role for the gene products in adhesion-mediated signalling. Analysis of a panel of breast tumour cell lines revealed that a number apparently overexpressed the gene whilst others showed very low levels of transcription. In one case, the overexpression correlated with a low level increase in gene copy number in the tumour line. In addition to differences in the overall levels of expression, LPHH1 mRNAs were alternatively spliced to varying degrees with shifts in the major gene product to truncated or altered forms in some lines. No somatic LPHH1 mutations were detected through sequence analysis of four primary breast tumours that showed loss of the adjacent 1p31.1 marker D1S207. (C) 2000 Elsevier Science B.V. All rights reserved.
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页码:75 / 92
页数:18
相关论文
共 16 条
[1]  
Bissell MJ, 1999, CANCER RES, V59, p1757S
[2]   Regulation of cell proliferation by G proteins [J].
Dhanasekaran, N ;
Tsim, ST ;
Dermott, JM ;
Onesime, D .
ONCOGENE, 1998, 17 (11) :1383-1394
[3]   ESTABLISHMENT AND CHARACTERIZATION OF A NEW TUMORIGENIC CELL-LINE WITH A NORMAL KARYOTYPE DERIVED FROM A HUMAN BREAST ADENOCARCINOMA [J].
GIOANNI, J ;
LEFRANCOIS, D ;
ZANGHELLINI, E ;
MAZEAU, C ;
ETTORE, F ;
LAMBERT, JC ;
SCHNEIDER, M ;
DUTRILLAUX, B .
BRITISH JOURNAL OF CANCER, 1990, 62 (01) :8-13
[4]   Cell growth control by G protein-coupled receptors: from signal transduction to signal integration [J].
Gutkind, JS .
ONCOGENE, 1998, 17 (11) :1331-1342
[5]   Coamplification in tumors of KRAS2, type 2 inositol 1,4,5 triphosphate receptor gene, and a novel human gene, KRAG [J].
Heighway, J ;
Betticher, DC ;
Hoban, PR ;
Altermatt, HJ ;
Cowen, R .
GENOMICS, 1996, 35 (01) :207-214
[6]   IDENTIFICATION AND CLONING IN YEAST ARTIFICIAL CHROMOSOMES OF A REGION OF ELEVATED LOSS OF HETEROZYGOSITY ON CHROMOSOME 1P31.1 IN HUMAN BREAST-CANCER [J].
HOGGARD, N ;
HEY, Y ;
BRINTNELL, B ;
JAMES, L ;
JONES, D ;
MITCHELL, E ;
WEISSENBACH, J ;
VARLEY, JM .
GENOMICS, 1995, 30 (02) :233-243
[7]   A novel ubiquitously expressed α-latrotoxin receptor is a member of the CIRL family of G-protein-coupled receptors [J].
Ichtchenko, K ;
Bittner, MA ;
Krasnoperov, V ;
Little, AR ;
Chepurny, O ;
Holz, RW ;
Petrenko, AG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (09) :5491-5498
[8]  
Journot Laurent, 1994, Seminars in Cell Biology, V5, P263, DOI 10.1006/scel.1994.1032
[9]   alpha-latrotoxin stimulates exocytosis by the interaction with a neuronal G-protein-coupled receptor [J].
Krasnoperov, VG ;
Bittner, MA ;
Beavis, R ;
Kuang, YN ;
Salnikow, KV ;
Chepurny, OG ;
Little, AR ;
Plotnikov, AN ;
Wu, DQ ;
Holz, RW ;
Petrenko, AG .
NEURON, 1997, 18 (06) :925-937
[10]   alpha-Latrotoxin receptor, latrophilin, is a novel member of the secretin family of G protein-coupled receptors [J].
Lelianova, VG ;
Davletov, BA ;
Sterling, A ;
Rahman, MA ;
Grishin, EV ;
Totty, NF ;
Ushkaryov, YA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (34) :21504-21508