Germline mutations in the RB1 gene in patients with hereditary retinoblastoma

Zaoxia Liu, Yue Song, Britta Bia, John Kenneth Cowell

Research output: Contribution to journalArticle

25 Citations (Scopus)

Abstract

We have analyzed the 27 exons and the promoter region of the RB1 gene in familial or sporadic bilateral retinoblastoma by using single‐strand conformation polymorphism analysis. For improvement over previous studies, a new set of primers has been designed, which allow for amplification of the coding and splicing sequences only. The positioning of the polymerase chain reaction (PCR) primers was such that the resulting PCR products were of different sizes, which enabled us to analyze two different exons simultaneously and still distinguish between the banding profiles for both (biplex analysis). By using this approach, we were able to identify mutations in 22 new patients, but the overall efficiency of the procedure when we used a single‐pass regimen was only 48%. The mutations were small insertions and deletions and point mutations in roughly equal proportions.

Original languageEnglish (US)
Pages (from-to)277-284
Number of pages8
JournalGenes, Chromosomes and Cancer
Volume14
Issue number4
DOIs
StatePublished - Dec 1995
Externally publishedYes

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Retinoblastoma
Germ-Line Mutation
Exons
INDEL Mutation
Polymerase Chain Reaction
Mutation
Point Mutation
Genetic Promoter Regions
Genes

ASJC Scopus subject areas

  • Genetics
  • Cancer Research

Cite this

Germline mutations in the RB1 gene in patients with hereditary retinoblastoma. / Liu, Zaoxia; Song, Yue; Bia, Britta; Cowell, John Kenneth.

In: Genes, Chromosomes and Cancer, Vol. 14, No. 4, 12.1995, p. 277-284.

Research output: Contribution to journalArticle

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