Literature DB >> 18347820

Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation.

Ana B Rodríguez-Martínez1, Miguel A Alfonso-Sánchez, José A Peña, Raquel Sánchez-Valle, Inga Zerr, Sabina Capellari, Miguel Calero, Juan J Zarranz, Marian M de Pancorbo.   

Abstract

This work presents a detailed investigation of the genomic region surrounding the PRNP gene in a sample of patients diagnosed with fatal familial insomnia (FFI) from several European countries, notably Spain. The main focus of the study was to explore the origins of the chromosomes carrying the D178N mutation by designing a single-nucleotide polymorphism (SNP) haplotype around the PRNP gene. Haplotypes were constructed by genotyping six SNPs (rs2756271, rs13040327, rs6037932, rs13045348, rs6116474, and rs6116475) in 25 FFI patients from all over Spain. To augment the geographical scope of our study, 13 further FFI cases from Germany (9) and Italy (4) were also examined. Genotyping of SNPs in conjunction with the analysis of genealogical data for a group of FFI patients revealed the existence of two distinct haplotypes potentially associated with the D178N mutation. Of them, GCATTA-M proved to be the common haplotype of Spanish patients, whereas ACATTA-M was typical of the German cases. It is interesting to note that both haplotypes were identified in the Italian samples: GCATTA-M in a family from the Tuscany region and ACATTA-M in a family from the Veneto region. Our findings suggest the occurrence of two independent D178N-129M mutational events in Europe, preserved and transmitted from one generation to the next until nowadays. Likewise, results based on the analysis of SNP data indicate that previous hypotheses postulating that the D178N mutation had independent origins for each family and that its global distribution was determined by recurrent mutational events must be regarded with caution.

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Year:  2008        PMID: 18347820     DOI: 10.1007/s10048-008-0120-x

Source DB:  PubMed          Journal:  Neurogenetics        ISSN: 1364-6745            Impact factor:   2.660


  39 in total

1.  Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia.

Authors:  Y Taniwaki; H Hara; K Doh-Ura; I Murakami; H Tashiro; T Yamasaki; H Shigeto; K Arakawa; E Araki; T Yamada; T Iwaki; J Kira
Journal:  J Neurol Neurosurg Psychiatry       Date:  2000-03       Impact factor: 10.154

2.  Single nucleotide polymorphisms. From the evolutionary past...

Authors:  M Stoneking
Journal:  Nature       Date:  2001-02-15       Impact factor: 49.962

3.  Age and origin of the PRNP E200K mutation causing familial Creutzfeldt-Jacob disease in Libyan Jews.

Authors:  R Colombo
Journal:  Am J Hum Genet       Date:  2000-08       Impact factor: 11.025

4.  The D178N (cis-129M) "fatal familial insomnia" mutation associated with diverse clinicopathologic phenotypes in an Australian kindred.

Authors:  C A McLean; E Storey; R J Gardner; A E Tannenberg; L Cervenáková; P Brown
Journal:  Neurology       Date:  1997-08       Impact factor: 9.910

5.  Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy.

Authors:  Ayush Dagvadorj; Robert B Petersen; Hee Suk Lee; Larisa Cervenakova; Alexey Shatunov; Herbert Budka; Paul Brown; Pierluigi Gambetti; Lev G Goldfarb
Journal:  Ann Neurol       Date:  2002-09       Impact factor: 10.422

6.  Genetic prion disease: the EUROCJD experience.

Authors:  Gábor G Kovács; Maria Puopolo; Anna Ladogana; Maurizio Pocchiari; Herbert Budka; Cornelia van Duijn; Steven J Collins; Alison Boyd; Antonio Giulivi; Mike Coulthart; Nicole Delasnerie-Laupretre; Jean Philippe Brandel; Inga Zerr; Hans A Kretzschmar; Jesus de Pedro-Cuesta; Miguel Calero-Lara; Markus Glatzel; Adriano Aguzzi; Matthew Bishop; Richard Knight; Girma Belay; Robert Will; Eva Mitrova
Journal:  Hum Genet       Date:  2005-11-15       Impact factor: 4.132

7.  Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene.

Authors:  R Medori; H J Tritschler; A LeBlanc; F Villare; V Manetto; H Y Chen; R Xue; S Leal; P Montagna; P Cortelli
Journal:  N Engl J Med       Date:  1992-02-13       Impact factor: 91.245

8.  Phenotypic variability in fatal familial insomnia (D178N-129M) genotype.

Authors:  I Zerr; A Giese; O Windl; S Kropp; W Schulz-Schaeffer; C Riedemann; K Skworc; M Bodemer; H A Kretzschmar; S Poser
Journal:  Neurology       Date:  1998-11       Impact factor: 9.910

9.  Clinical features of fatal familial insomnia: phenotypic variability in relation to a polymorphism at codon 129 of the prion protein gene.

Authors:  P Montagna; P Cortelli; P Avoni; P Tinuper; G Plazzi; R Gallassi; F Portaluppi; J Julien; C Vital; M B Delisle; P Gambetti; E Lugaresi
Journal:  Brain Pathol       Date:  1998-07       Impact factor: 6.508

Review 10.  Molecular pathology of fatal familial insomnia.

Authors:  P Parchi; R B Petersen; S G Chen; L Autilio-Gambetti; S Capellari; L Monari; P Cortelli; P Montagna; E Lugaresi; P Gambetti
Journal:  Brain Pathol       Date:  1998-07       Impact factor: 6.508

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  4 in total

1.  Global distribution of fatal familial insomnia: founder or recurrent mutations.

Authors:  H-S Lee; L G Goldfarb
Journal:  Neurogenetics       Date:  2008-06-21       Impact factor: 2.660

2.  Genotype patterns and characteristics of PRNP in the Korean population.

Authors:  Sol Moe Lee; Young Ran Ju; Bo-Yeong Choi; Jae Wook Hyeon; Jun Sun Park; Chi Kyeong Kim; Su Yeon Kim
Journal:  Prion       Date:  2012-05-07       Impact factor: 3.931

3.  Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain.

Authors:  Ignacio F Mata; Carolyn M Hutter; María C González-Fernández; Marian M de Pancorbo; Elena Lezcano; Cecilia Huerta; Marta Blazquez; Renee Ribacoba; Luis M Guisasola; Carlos Salvador; Juan C Gómez-Esteban; Juan J Zarranz; Jon Infante; Joseph Jankovic; Hao Deng; Karen L Edwards; Victoria Alvarez; Cyrus P Zabetian
Journal:  Neurogenetics       Date:  2009-03-24       Impact factor: 2.660

4.  Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing.

Authors:  Nadège Calmels; Géraldine Greff; Cathy Obringer; Nadine Kempf; Claire Gasnier; Julien Tarabeux; Marguerite Miguet; Geneviève Baujat; Didier Bessis; Patricia Bretones; Anne Cavau; Béatrice Digeon; Martine Doco-Fenzy; Bérénice Doray; François Feillet; Jesus Gardeazabal; Blanca Gener; Sophie Julia; Isabel Llano-Rivas; Artur Mazur; Caroline Michot; Florence Renaldo-Robin; Massimiliano Rossi; Pascal Sabouraud; Boris Keren; Christel Depienne; Jean Muller; Jean-Louis Mandel; Vincent Laugel
Journal:  Orphanet J Rare Dis       Date:  2016-03-22       Impact factor: 4.123

  4 in total

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