Mendelian diseases among Roman Jews: Implications for the origins of disease alleles

Carole Oddoux, Encarnacion Guillen-Navarro, Claudio Ditivoli, Elvira Dicave, Maria Roberta Cilio, C. Mark Clayton, Holly Nelson, Kyriakie Sarafoglou, Nicole McCain, Hava Peretz, Uri Seligsohn, Lucio Luzzatto, Khedouja Nafa, Michael Nardi, Margaret Karpatkin, Ivona Aksentijevich, Daniel Kastner, Felicia Axelrod, Harry Ostrer

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

The Roman Jewish community has been historically continuous in Rome since pre-Christian times and may have been progenitor to the Ashkenazi Jewish community. Despite a history of endogamy over the past 2000 yr, the historical record suggests that there was admixture with Ashkenazi and Sephardic Jews during the Middle Ages. To determine whether Roman and Ashkenazi Jews shared common signature mutations, we tested a group of 107 Roman Jews, representing 176 haploid sets of chromosomes. No mutations were found for Bloom syndrome, BRCA1, BRCA2, Canavan disease, Fanconi anemia complementation group C, or Tay-Sachs disease. Two unrelated individuals were positive for the 3849 + 10C->T cystic fibrosis mutation; one carried the N370S Gaucher disease mutation, and one carried the connexin 26 167delT mutation. Each of these was shown to be associated with the same haplotype of tightly linked microsatellite markers as that found among Ashkenazi Jews. In addition, 14 individuals had mutations in the familial Mediterranean fever gene and three unrelated individuals carried the factor XI type III mutation previously observed exclusively among Ashkenazi Jews. These findings suggest that the Gaucher, connexin 26, and familial Mediterranean fever mutations are over 2000 yr old, that the cystic fibrosis 3849 + 10kb C->T and factor XI type III mutations had a common origin in Ashkenazi and Roman Jews, and that other mutations prevalent among Ashkenazi Jews are of more recent origin.

Original languageEnglish (US)
Pages (from-to)4405-4409
Number of pages5
JournalJournal of Clinical Endocrinology and Metabolism
Volume84
Issue number12
StatePublished - 1999
Externally publishedYes

Fingerprint

Jews
Factor XI
Connexins
Alleles
Mutation
Chromosomes
Microsatellite Repeats
Familial Mediterranean Fever
Genes
Cystic Fibrosis
Canavan Disease
Bloom Syndrome
Tay-Sachs Disease
Fanconi Anemia
Gaucher Disease
Haploidy
Haplotypes

ASJC Scopus subject areas

  • Biochemistry
  • Endocrinology, Diabetes and Metabolism

Cite this

Oddoux, C., Guillen-Navarro, E., Ditivoli, C., Dicave, E., Cilio, M. R., Clayton, C. M., ... Ostrer, H. (1999). Mendelian diseases among Roman Jews: Implications for the origins of disease alleles. Journal of Clinical Endocrinology and Metabolism, 84(12), 4405-4409.

Mendelian diseases among Roman Jews : Implications for the origins of disease alleles. / Oddoux, Carole; Guillen-Navarro, Encarnacion; Ditivoli, Claudio; Dicave, Elvira; Cilio, Maria Roberta; Clayton, C. Mark; Nelson, Holly; Sarafoglou, Kyriakie; McCain, Nicole; Peretz, Hava; Seligsohn, Uri; Luzzatto, Lucio; Nafa, Khedouja; Nardi, Michael; Karpatkin, Margaret; Aksentijevich, Ivona; Kastner, Daniel; Axelrod, Felicia; Ostrer, Harry.

In: Journal of Clinical Endocrinology and Metabolism, Vol. 84, No. 12, 1999, p. 4405-4409.

Research output: Contribution to journalArticle

Oddoux, C, Guillen-Navarro, E, Ditivoli, C, Dicave, E, Cilio, MR, Clayton, CM, Nelson, H, Sarafoglou, K, McCain, N, Peretz, H, Seligsohn, U, Luzzatto, L, Nafa, K, Nardi, M, Karpatkin, M, Aksentijevich, I, Kastner, D, Axelrod, F & Ostrer, H 1999, 'Mendelian diseases among Roman Jews: Implications for the origins of disease alleles', Journal of Clinical Endocrinology and Metabolism, vol. 84, no. 12, pp. 4405-4409.
Oddoux C, Guillen-Navarro E, Ditivoli C, Dicave E, Cilio MR, Clayton CM et al. Mendelian diseases among Roman Jews: Implications for the origins of disease alleles. Journal of Clinical Endocrinology and Metabolism. 1999;84(12):4405-4409.
Oddoux, Carole ; Guillen-Navarro, Encarnacion ; Ditivoli, Claudio ; Dicave, Elvira ; Cilio, Maria Roberta ; Clayton, C. Mark ; Nelson, Holly ; Sarafoglou, Kyriakie ; McCain, Nicole ; Peretz, Hava ; Seligsohn, Uri ; Luzzatto, Lucio ; Nafa, Khedouja ; Nardi, Michael ; Karpatkin, Margaret ; Aksentijevich, Ivona ; Kastner, Daniel ; Axelrod, Felicia ; Ostrer, Harry. / Mendelian diseases among Roman Jews : Implications for the origins of disease alleles. In: Journal of Clinical Endocrinology and Metabolism. 1999 ; Vol. 84, No. 12. pp. 4405-4409.
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