Cancer-specific chromosome alterations in the constitutive fragile region FRA3B

Koshi Mimori, Teresa Druck, Hiroshi Inoue, Hansjuerg Alder, Lori Berk, Masaki Mori, Kay Huebner, Carlo M. Croce

研究成果: ジャーナルへの寄稿記事

119 引用 (Scopus)

抄録

We have sequenced 870 kilobases of the FHIT/FRA3B locus, from FHIT intron 3 to intron 7. The locus is AT rich (61.5%) and Alu poor (6.2%), and it apparently does not harbor other genes. In a detailed analysis of the 308- kilobase region between FHIT exon 5 and the telomeric end of intron 3, a region known to encompass a human papillomavirus-16 integration site and two clusters of aphidicolin-induced chromosome 3p14.2 breakpoints, we have precisely mapped 10 deletion and translocation endpoints in cancer-derived cell lines relative to positions of specific repetitive elements, regions of high genome flexibility and aphidicolin-induced breakpoints. Conclusions are (i) that aphidicolin-induced breakpoint clusters fall close to high- flexibility sequences, suggesting that these sequences contribute directly to aphidicolin-induced fragility; (ii) that 9 of the 10 FH1T allelic deletions in cancer cell lines resulted in loss of exons, with 7 deletion endpoints near long interspersed nuclear elements or long terminal repeat elements; and (iii) that cancer-specific deletions encompass multiple high-flexibility genomic regions, suggesting that fragile breaks may occur at these regions, whereas repair of the breaks involves homologous pairing of flanking sequences with concomitant deletion of the damaged fragile sequence.

元の言語英語
ページ(範囲)7456-7461
ページ数6
ジャーナルProceedings of the National Academy of Sciences of the United States of America
96
発行部数13
DOI
出版物ステータス出版済み - 6 22 1999

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Aphidicolin
Chromosomes
Introns
Exons
Neoplasms
Chromosome Breakpoints
Cell Line
Human papillomavirus 16
Terminal Repeat Sequences
Nucleic Acid Repetitive Sequences
Genome
Genes

All Science Journal Classification (ASJC) codes

  • General

これを引用

Cancer-specific chromosome alterations in the constitutive fragile region FRA3B. / Mimori, Koshi; Druck, Teresa; Inoue, Hiroshi; Alder, Hansjuerg; Berk, Lori; Mori, Masaki; Huebner, Kay; Croce, Carlo M.

:: Proceedings of the National Academy of Sciences of the United States of America, 巻 96, 番号 13, 22.06.1999, p. 7456-7461.

研究成果: ジャーナルへの寄稿記事

Mimori, Koshi ; Druck, Teresa ; Inoue, Hiroshi ; Alder, Hansjuerg ; Berk, Lori ; Mori, Masaki ; Huebner, Kay ; Croce, Carlo M. / Cancer-specific chromosome alterations in the constitutive fragile region FRA3B. :: Proceedings of the National Academy of Sciences of the United States of America. 1999 ; 巻 96, 番号 13. pp. 7456-7461.
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abstract = "We have sequenced 870 kilobases of the FHIT/FRA3B locus, from FHIT intron 3 to intron 7. The locus is AT rich (61.5{\%}) and Alu poor (6.2{\%}), and it apparently does not harbor other genes. In a detailed analysis of the 308- kilobase region between FHIT exon 5 and the telomeric end of intron 3, a region known to encompass a human papillomavirus-16 integration site and two clusters of aphidicolin-induced chromosome 3p14.2 breakpoints, we have precisely mapped 10 deletion and translocation endpoints in cancer-derived cell lines relative to positions of specific repetitive elements, regions of high genome flexibility and aphidicolin-induced breakpoints. Conclusions are (i) that aphidicolin-induced breakpoint clusters fall close to high- flexibility sequences, suggesting that these sequences contribute directly to aphidicolin-induced fragility; (ii) that 9 of the 10 FH1T allelic deletions in cancer cell lines resulted in loss of exons, with 7 deletion endpoints near long interspersed nuclear elements or long terminal repeat elements; and (iii) that cancer-specific deletions encompass multiple high-flexibility genomic regions, suggesting that fragile breaks may occur at these regions, whereas repair of the breaks involves homologous pairing of flanking sequences with concomitant deletion of the damaged fragile sequence.",
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AU - Mimori, Koshi

AU - Druck, Teresa

AU - Inoue, Hiroshi

AU - Alder, Hansjuerg

AU - Berk, Lori

AU - Mori, Masaki

AU - Huebner, Kay

AU - Croce, Carlo M.

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N2 - We have sequenced 870 kilobases of the FHIT/FRA3B locus, from FHIT intron 3 to intron 7. The locus is AT rich (61.5%) and Alu poor (6.2%), and it apparently does not harbor other genes. In a detailed analysis of the 308- kilobase region between FHIT exon 5 and the telomeric end of intron 3, a region known to encompass a human papillomavirus-16 integration site and two clusters of aphidicolin-induced chromosome 3p14.2 breakpoints, we have precisely mapped 10 deletion and translocation endpoints in cancer-derived cell lines relative to positions of specific repetitive elements, regions of high genome flexibility and aphidicolin-induced breakpoints. Conclusions are (i) that aphidicolin-induced breakpoint clusters fall close to high- flexibility sequences, suggesting that these sequences contribute directly to aphidicolin-induced fragility; (ii) that 9 of the 10 FH1T allelic deletions in cancer cell lines resulted in loss of exons, with 7 deletion endpoints near long interspersed nuclear elements or long terminal repeat elements; and (iii) that cancer-specific deletions encompass multiple high-flexibility genomic regions, suggesting that fragile breaks may occur at these regions, whereas repair of the breaks involves homologous pairing of flanking sequences with concomitant deletion of the damaged fragile sequence.

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