Genomic organization, comparative analysis, and genetic polymorphisms of the bovine and ovine prion Doppel genes (PRND)

被引:47
作者
Comincini, S
Foti, MG
Tranulis, MA
Hills, D
Di Guardo, G
Vaccari, G
Williams, JL
Harbitz, I
Ferretti, L
机构
[1] Univ Pavia, Dipartimento Genet & Microbiol, I-27100 Pavia, Italy
[2] Norwegian Sch Vet Sci, Oslo, Norway
[3] Roslin Inst, Roslin EH25 9PS, Midlothian, Scotland
[4] Ist Zooprofilatt Sperimantale Reg Lazio & Toscana, Rome, Italy
[5] Ist Super Sanita, Lab Med Vet, I-00161 Rome, Italy
关键词
D O I
10.1007/s00335-001-2064-4
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 doppel protein (Dpl) is a prion-like protein encoded by the gene PRND, which has been found downstream of the prion gene, PRNP, in human and mouse. This paper describes the isolation and structural organization of the bovine and ovine PRND genes, which are composed of two exons compared with the three of human and mouse. Intergenic distances between PRNP and PRND were covered by means of long-range PCR and found to be 16.8 and 20 kb, in cattle and sheep respectively. The 5' and 3' untranslated regions (UTR) were analyzed to identify transcription regulatory sequences and compared with those from the PRND and PRNP sequences published for other species. Three polymorphisms (R50H, N110H, and R132Q) were revealed in the cattle coding region; two synonymous substitutions (I12I, A26A) were found in sheep. None of the polymorphisms was significantly associated with either Bovine Spongiform. Encephalopathy (BSE) in cattle or scrapie in sheep.
引用
收藏
页码:729 / 733
页数:5
相关论文
共 18 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   Comparative mapping of the prion gene (PRNP) locus in cattle, sheep and human with PCR-generated probes [J].
Castiglioni, B ;
Comincini, S ;
Drisaldi, B ;
Motta, T ;
Ferretti, L .
MAMMALIAN GENOME, 1998, 9 (10) :853-855
[3]  
Comincini S., 2000, Current Genomics, V1, P313, DOI 10.2174/1389202003351274
[4]   PrP (prion) gene expression in sheep may be modulated by alternative polyadenylation of its messenger RNA [J].
Goldmann, W ;
O'Neill, G ;
Cheung, F ;
Charleson, F ;
Ford, P ;
Hunter, N .
JOURNAL OF GENERAL VIROLOGY, 1999, 80 :2275-2283
[5]   Scrapie [J].
Hunter, N .
MOLECULAR BIOTECHNOLOGY, 1998, 9 (03) :225-234
[6]   FREQUENCIES OF PRP GENE VARIANTS IN HEALTHY CATTLE AND CATTLE WITH BSE IN SCOTLAND [J].
HUNTER, N ;
GOLDMANN, W ;
SMITH, G ;
HOPE, J .
VETERINARY RECORD, 1994, 135 (17) :400-403
[7]   Complete genomic sequence and analysis of the prion protein gene region from three mammalian species [J].
Lee, IY ;
Westaway, D ;
Smit, AFA ;
Wang, K ;
Seto, J ;
Chen, L ;
Acharya, C ;
Ankener, M ;
Baskin, D ;
Cooper, C ;
Yao, H ;
Prusiner, SB ;
Hood, LE .
GENOME RESEARCH, 1998, 8 (10) :1022-1037
[8]   Examination of the human prion protein-like gene Doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease [J].
Mead, S ;
Beck, J ;
Dickinson, A ;
Fisher, EMC ;
Collinge, J .
NEUROSCIENCE LETTERS, 2000, 290 (02) :117-120
[9]   Ataxia in prion protein (PrP)-deficient mice is associated with upregulation of the novel PrP-like protein Doppel [J].
Moore, RC ;
Lee, IY ;
Silverman, GL ;
Harrison, PM ;
Strome, R ;
Heinrich, C ;
Karunaratne, A ;
Pasternak, SH ;
Chishti, MA ;
Liang, Y ;
Mastrangelo, P ;
Wang, K ;
Smit, AFA ;
Katamine, S ;
Carlson, GA ;
Cohen, FE ;
Prusiner, SB ;
Melton, DW ;
Tremblay, P ;
Hood, LE ;
Westaway, D .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 292 (04) :797-817
[10]   First report of polymorphisms in the prion-like protein gene (PRND):: implications for human prion diseases [J].
Peoc'h, K ;
Guérin, C ;
Brandel, JP ;
Launay, JM ;
Laplanche, JL .
NEUROSCIENCE LETTERS, 2000, 286 (02) :144-148