Prenatal diagnosis of a rhodopsin mutation using chemical cleavage of the mismatch

Alessandra Tessitore, Elena Toniato, Alberto Gulino, Luigi Frati, Enrico Ricevuto, Maria Vadal, Enzo Vingolo, Stefano Martinotti

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Objective: Mutations of the rhodopsin gene are responsible for autosomal dominant or recessive retinitis pigmentosa (RP). The present study reports the first prenatal diagnosis performed on chorionic villi biopsy of a pregnant woman affected by a severe form of autosomal dominant transmitted RP, due to the Arg135Trp substitution. Methods: The rhodopsin gene was analysed by automated direct sequencing and, for the first time, by fluorescence-assisted mismatch analysis (FAMA). The latter is an inexpensive, rapid and particularly sensitive method, based on the chemical cleavage of the mismatch in heteroduplex DNA molecules marked with strand-specific fluorophores. Results: FAMA is a feasible procedure for prenatal molecular diagnosis of rhodopsin mutations. The redundancy of signals obtained by FAMA and its sensitivity make it suitable for identifying exactly the position of the mutation and the nucleotide substitution. Conclusions: An association is proposed between FAMA and automated direct sequencing procedures, in order to achieve optimal results in terms of reliability for prenatal diagnosis of rhodopsin mutations.

Original languageEnglish
Pages (from-to)380-384
Number of pages5
JournalPrenatal Diagnosis
Volume22
Issue number5
DOIs
Publication statusPublished - 2002

Fingerprint

Rhodopsin
Prenatal Diagnosis
Fluorescence
Mutation
Retinitis Pigmentosa
Nucleic Acid Heteroduplexes
Chorionic Villi Sampling
Genes
Pregnant Women
Nucleotides

Keywords

  • FAMA
  • Retinitis pigmentosa
  • Rhodopsin gene

ASJC Scopus subject areas

  • Genetics(clinical)
  • Obstetrics and Gynaecology

Cite this

Tessitore, A., Toniato, E., Gulino, A., Frati, L., Ricevuto, E., Vadal, M., ... Martinotti, S. (2002). Prenatal diagnosis of a rhodopsin mutation using chemical cleavage of the mismatch. Prenatal Diagnosis, 22(5), 380-384. https://doi.org/10.1002/pd.263

Prenatal diagnosis of a rhodopsin mutation using chemical cleavage of the mismatch. / Tessitore, Alessandra; Toniato, Elena; Gulino, Alberto; Frati, Luigi; Ricevuto, Enrico; Vadal, Maria; Vingolo, Enzo; Martinotti, Stefano.

In: Prenatal Diagnosis, Vol. 22, No. 5, 2002, p. 380-384.

Research output: Contribution to journalArticle

Tessitore, A, Toniato, E, Gulino, A, Frati, L, Ricevuto, E, Vadal, M, Vingolo, E & Martinotti, S 2002, 'Prenatal diagnosis of a rhodopsin mutation using chemical cleavage of the mismatch', Prenatal Diagnosis, vol. 22, no. 5, pp. 380-384. https://doi.org/10.1002/pd.263
Tessitore, Alessandra ; Toniato, Elena ; Gulino, Alberto ; Frati, Luigi ; Ricevuto, Enrico ; Vadal, Maria ; Vingolo, Enzo ; Martinotti, Stefano. / Prenatal diagnosis of a rhodopsin mutation using chemical cleavage of the mismatch. In: Prenatal Diagnosis. 2002 ; Vol. 22, No. 5. pp. 380-384.
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AU - Vadal, Maria

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