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- Publisher Website: 10.1016/j.febslet.2007.08.061
- Scopus: eid_2-s2.0-34548679388
- PMID: 17826769
- WOS: WOS:000250102900021
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Article: CpG/CpNpG motifs in the coding region are preferred sites for mutagenesis in the breast cancer susceptibility genes
Title | CpG/CpNpG motifs in the coding region are preferred sites for mutagenesis in the breast cancer susceptibility genes |
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Authors | |
Keywords | BRCA1 BRCA2 Breast cancer susceptibility gene Gene mutation |
Issue Date | 2007 |
Publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/febslet |
Citation | FEBS Letters, 2007, v. 581 n. 24, p. 4668-4674 How to Cite? |
Abstract | The range of BRCA1/BRCA2 gene mutations is diverse and the mechanism accounting for this heterogeneity is obscure. To gain insight into the endogenous mutational mechanisms involved, we evaluated the association of specific sequences (i.e. CpG/CpNpG motifs, homonucleotides, short repeats) and mutations within the genes. We classified 1337 published mutations in BRCA1 (1765 BRCA2 mutations) for each specific sequence, and employed computer simulation combined with mathematical calculations to estimate the true underlying tendency of mutation occurrence. Interestingly, we found no mutational bias to homonucleotides and repeats in deletions/insertions and substitutions but striking bias to CpG/CpNpG in substitutions in both genes. This suggests that methylation-dependent DNA alterations would be a major mechanism for mutagenesis. © 2007 Federation of European Biochemical Societies. |
Persistent Identifier | http://hdl.handle.net/10722/75377 |
ISSN | 2023 Impact Factor: 3.0 2023 SCImago Journal Rankings: 1.208 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Cheung, LWT | en_HK |
dc.contributor.author | Lee, YF | en_HK |
dc.contributor.author | Ng, TW | en_HK |
dc.contributor.author | Ching, WK | en_HK |
dc.contributor.author | Khoo, US | en_HK |
dc.contributor.author | Ng, MKP | en_HK |
dc.contributor.author | Wong, AST | en_HK |
dc.date.accessioned | 2010-09-06T07:10:32Z | - |
dc.date.available | 2010-09-06T07:10:32Z | - |
dc.date.issued | 2007 | en_HK |
dc.identifier.citation | FEBS Letters, 2007, v. 581 n. 24, p. 4668-4674 | en_HK |
dc.identifier.issn | 0014-5793 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/75377 | - |
dc.description.abstract | The range of BRCA1/BRCA2 gene mutations is diverse and the mechanism accounting for this heterogeneity is obscure. To gain insight into the endogenous mutational mechanisms involved, we evaluated the association of specific sequences (i.e. CpG/CpNpG motifs, homonucleotides, short repeats) and mutations within the genes. We classified 1337 published mutations in BRCA1 (1765 BRCA2 mutations) for each specific sequence, and employed computer simulation combined with mathematical calculations to estimate the true underlying tendency of mutation occurrence. Interestingly, we found no mutational bias to homonucleotides and repeats in deletions/insertions and substitutions but striking bias to CpG/CpNpG in substitutions in both genes. This suggests that methylation-dependent DNA alterations would be a major mechanism for mutagenesis. © 2007 Federation of European Biochemical Societies. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/febslet | en_HK |
dc.relation.ispartof | FEBS Letters | en_HK |
dc.subject | BRCA1 | en_HK |
dc.subject | BRCA2 | en_HK |
dc.subject | Breast cancer susceptibility gene | en_HK |
dc.subject | Gene mutation | en_HK |
dc.subject.mesh | BRCA1 Protein - genetics | - |
dc.subject.mesh | BRCA2 Protein - genetics | - |
dc.subject.mesh | Breast Neoplasms - genetics - pathology | - |
dc.subject.mesh | Genetic Predisposition to Disease - genetics | - |
dc.subject.mesh | Open Reading Frames - genetics | - |
dc.title | CpG/CpNpG motifs in the coding region are preferred sites for mutagenesis in the breast cancer susceptibility genes | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Ng, TW: ngtw@hku.hk | en_HK |
dc.identifier.email | Ching, WK: wching@hku.hk | en_HK |
dc.identifier.email | Khoo, US: uskhoo@hku.hk | en_HK |
dc.identifier.email | Wong, AST: awong1@hkucc.hku.hk | en_HK |
dc.identifier.authority | Ng, TW=rp00768 | en_HK |
dc.identifier.authority | Ching, WK=rp00679 | en_HK |
dc.identifier.authority | Khoo, US=rp00362 | en_HK |
dc.identifier.authority | Wong, AST=rp00805 | en_HK |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1016/j.febslet.2007.08.061 | en_HK |
dc.identifier.pmid | 17826769 | - |
dc.identifier.scopus | eid_2-s2.0-34548679388 | en_HK |
dc.identifier.hkuros | 138469 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-34548679388&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 581 | en_HK |
dc.identifier.issue | 24 | en_HK |
dc.identifier.spage | 4668 | en_HK |
dc.identifier.epage | 4674 | en_HK |
dc.identifier.isi | WOS:000250102900021 | - |
dc.publisher.place | Netherlands | en_HK |
dc.identifier.scopusauthorid | Cheung, LWT=14119560800 | en_HK |
dc.identifier.scopusauthorid | Lee, YF=14527155400 | en_HK |
dc.identifier.scopusauthorid | Ng, TW=7402229732 | en_HK |
dc.identifier.scopusauthorid | Ching, WK=13310265500 | en_HK |
dc.identifier.scopusauthorid | Khoo, US=7004195799 | en_HK |
dc.identifier.scopusauthorid | Ng, MKP=34571761900 | en_HK |
dc.identifier.scopusauthorid | Wong, AST=23987963300 | en_HK |
dc.identifier.issnl | 0014-5793 | - |