Literature DB >> 8416016

Search for a genetic event in monozygotic twins discordant for schizophrenia.

M H Polymeropoulos1, H Xiao, E F Torrey, L E DeLisi, T Crow, C R Merril.   

Abstract

When monozygotic twins are discordant for the diagnosis of schizophrenia, this discordance has been traditionally attributed to environmental factors acting upon a genome susceptible for the schizophrenia phenotype. The study presented here was designed to examine the occurrence of a genetic event, such as a postzygotic mitotic crossover, that could account for the discordance. Such a postzygotic event could affect cis-acting sequences and result in a phenotype of variable severity. We used molecular genetic methods to evaluate such an event with 94 microsatellite repeat polymorphic markers distributed on all autosomes and the X chromosome in five pairs of monozygotic twins discordant for schizophrenia. In this search, no genetic marker discordances were identified between the co-twins. The lack of a genetic difference may implicate nongenetic factors that are responsible in eliciting or suppressing the phenotype. However, the experiments performed in this study cannot eliminate the possibility that a tissue-specific mitotic crossover might have occurred in one of the discordant twins, which could not have been detected in our current study.

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Year:  1993        PMID: 8416016     DOI: 10.1016/0165-1781(93)90110-3

Source DB:  PubMed          Journal:  Psychiatry Res        ISSN: 0165-1781            Impact factor:   3.222


  4 in total

1.  Autosomal recessive Wolfram syndrome associated with an 8.5-kb mtDNA single deletion.

Authors:  A Barrientos; J Casademont; A Saiz; F Cardellach; V Volpini; A Solans; E Tolosa; A Urbano-Marquez; X Estivill; V Nunes
Journal:  Am J Hum Genet       Date:  1996-05       Impact factor: 11.025

2.  Comparative diagnoses of twin zygosity by SSLP variant analysis, questionnaire, and dermatoglyphic analysis.

Authors:  E Spitz; R Moutier; T Reed; M C Busnel; C Marchaland; P L Roubertoux; M Carlier
Journal:  Behav Genet       Date:  1996-01       Impact factor: 2.805

3.  A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome.

Authors:  A Barrientos; V Volpini; J Casademont; D Genís; J M Manzanares; I Ferrer; J Corral; F Cardellach; A Urbano-Márquez; X Estivill; V Nunes
Journal:  J Clin Invest       Date:  1996-04-01       Impact factor: 14.808

Review 4.  Genetic and environmental factors of schizophrenia and autism spectrum disorder: insights from twin studies.

Authors:  Akira Imamura; Yoshiro Morimoto; Shinji Ono; Naohiro Kurotaki; Shinji Kanegae; Naoki Yamamoto; Hirohisa Kinoshita; Takahiro Tsujita; Yuji Okazaki; Hiroki Ozawa
Journal:  J Neural Transm (Vienna)       Date:  2020-04-13       Impact factor: 3.575

  4 in total

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