Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.788616
Title: Evaluation and application of screening strategies for point mutations in the retinoblastoma gene
Author: Dundar, Munis
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 1994
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Abstract:
The present study aimed to evaluate two screening strategies, single strand conformation polymorphism (SSCP) and amplification mismatch detection (AMD) analysis, for the detection of point mutations in the retinoblastoma gene (RB). SSCP was optimised and applied to exons 12-22 of the RB gene which constitute the most important functional domain. Leukocyte DNA from 20 patients with bilateral retinoblastoma (Rb), tumour DNA from 40 patients with bladder carcinoma and tumour DNA from 39 patients with breast carcinoma were subjected to SSCP analysis. SSCP band shifts were found in 4 of 20, 1 of 40 and none of 39 patients respectively. AMD was optimised and applied to exons 12-16 of the RB gene and also to reverse-transcriptase PCR in the 20 patients with bilateral Rb. Cleavage was found in 2 patients; one was found in a cDNA segment and the other was found in genomic DNA. Neither of these patients corresponded to the 4 with SSCP band shifts. Thus in total, 6 patients with Rb and one with bladder carcinoma had mutations detected and proof was sought by sequencing. Amplification of segment C of the cDNA of patients with bilateral Rb has revealed that patient EAS showed an additional band indicating either a deletion or a splice mutation. Analysis of exon 17 and the flanking intron of the same patient with AMD showed a cleavage with hydroxylamine. Sequencing of the exon revealed that the mutation is a C substitution of the A at position -2 of the acceptor site of intron 16, impairing normal splicing of the RNA. The mutation results in skipping of exon 17, because the short transcript band on the agarose gel was approximately 196 bp shorter than the original band and exon 17 was 196 bp in size. This leads in turn to the production of a truncated RB protein. By analogy to other published mutations, this aberrant, destabilised protein might not be able to bind the E1A oncoprotein. In addition, the mutant RB protein may fail to complex with SV40 large T antigen. Analysis of segment C of the cDNA from patient PC with bilateral Rb showed a cleavage with hydroxylamine reaction. Sequencing of the segment revealed the mutation to be a T→G transversion at nucleotide position 1587 within exon 16 causing a substitution of histidine to glycine. The missense mutation may or may not have a functional effect. However, this residue lies within an RB domain (aminoacids 393-572) identified recently by in vitro deletion mutants to be required for oncoprotein binding. This mutation creates a restriction site for Nde I. Sequencing of exon 21 from patient MH who had an SSCP band shift, revealed that an insertion of a G at nucleotide position 2251 within exon 21 resulted in a novel stop codon (TAA) at codon 719 (nucleotide position 2295) within exon 21 thus deleting the domain interacting with the SV40 T antigen. The translated protein is most probably too short to be functional. To confirm whether the observed SSCP pattern in the region of exon 21 of the RB gene was a new germ line mutation or inherited from one of the parents, heteroduplex analysis of the parents revealed either the mutation was de novo or one of the parents had germ line mosaicism. In addition, the change creates a restriction site for the restriction enzyme FokI. Another mutation detected (from patient AR) by SSCP analysis was an A to C transversion at position 1636 in exon 16 causing AGA to CGA codon change, both coding for the same amino acid: Arginine, this mutation abolishes a restriction site for the restriction enzyme CvijI. The mutation site was located in the last base of the exon 16, although it has not been shown in this study in mRNA, it could affect splicing of the mRNA of RB gene. Two mutations found were considered to be silent mutations, because they do not cause any amino acid change. Their RNA transcripts were found to be normal. These mutations were a T to C transition at position 1617 in exon 16 (Patient GM) which alters the codon GTT (GUU) to GTC (GUC) both coding for the same amino acid; Valine and an A→G transition in intron 19 (patient EAS) which abolishes a restriction site for the restriction enzyme Tsp 509 I which may be useful in tracking this mutation in affected family members. Analysis of 100 samples (patients with bilateral Rb and other tumours) for this restriction site revealed that none of them has same change. The mutation found from the patient with bladder carcinoma was a G to C transversion at position +1 of the donor site of intron 12, probably impairing normal splicing of the RNA. The second mutation was assumed to lie in a part of the retinoblastoma gene that was not analysed, since in somatic cases two hits in the RB gene are expected. Intact RNA could not always be recovered from the clinical material used in this study, therefore the diagnostic strategy for bladder carcinoma was chosen not to be based on the analysis of RNA transcript. The change creates a recognition site for the restriction enzymes MaeII, Bpu101, DdeI. The seven mutations detected in this study were all novel and emphasise the heterogeneity of the molecular pathology in this gene.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.788616  DOI: Not available
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