Strain-dependent developmental relaxation of imprinting of an endogenous mouse gene, K(v)lqt1

Genomics

Volumn 53, Issue 3, 1998, Pages 395-399

  Jiang, Shan ^a   Hemann, Michael A ^a   Lee, Maxwell P ^a   Feinberg, Andrew P ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELISM; ARTICLE; CHROMOSOME 15; CHROMOSOME REARRANGEMENT; EMBRYO DEVELOPMENT; GENETIC POLYMORPHISM; GENOME IMPRINTING; MOUSE; NONHUMAN; PRIORITY JOURNAL; STRAIN DIFFERENCE;

MUS; MUS MUSCULUS CASTANEUS; MUSCULUS; RODENTIA;

EID: 18744429099     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1998.5511     Document Type: Article

References (27)

1. Bepler G., Garcia-Blanco M. Three tumor-suppressor regions on chromosome 11p identified by high-resolution deletion mapping in human non-small-cell lung cancer. Proc. Natl. Acad. Sci. USA. 91:1994;5513-5517.
2. Chaillet J. R. Genomic imprinting: Lessons from mouse transgenes. Mutat. Res. 307:1996;441-449.
3. Chung W. Y., Yuan L., Feng L., Hensle T., Tycko B. Chromosome 11p15.5 regional imprinting - Comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors. Hum. Mol. Genet. 5:1996;1101-1108.
4. Feinberg A. P. A developmental context for multiple genetic alterations in Wilms' tumors. J. Cell Sci. 18:1994;7-12.
5. Feinberg A. P. Genomic imprinting and cancer. The Genetic Basis of Human Cancer. 1998;McGraw-Hill, New York. p. 95-107.
6. KIP2. Nat. Genet. 14:1996;171-173.
7. Hoovers J. M. N., Kalikin L. M., Johnson L. A., Alders M., Redeker B., Law D. J., Bliek J., Steenman M., Benedict M. et al. Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. Proc. Natl. Acad. Sci. USA. 92:1995;12456-12460.
8. Koufos A., Grundy P., Morgan K., Aleck K. A., Hadro T., Lampkin B. C., Kalbakji A., Cavenee W. K. Familial Beckwith-Wiedemann syndrome and a second Wilms' tumor locus both map to 11p15.5. Am. J. Hum. Genet. 44:1989;711-719.
9. KIP2. Am. J. Hum. Genet. 61:1997;304-309.
10. Lee M. P., Hu R., Johnson L. A., Feinberg A. P. Human KVlqt1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements. Nat. Genet. 15:1997;181-185.
11. KIP2. Proc. Natl. Acad. Sci. USA. 93:1996;3026-3030.
12. Moulton T., Crenshaw T., Hao Y., Moosikasuwan J., Lin N., Dembitzer F., Hensle T., Weiss L., McMorrow L., Loew T., Kraus W., Gerald W., Tycko B. Epigenetic lesions at the H19 locus in Wilms' tumor patients. Nat. Genet. 7:1994;440-447.
13. Ogawa O., Eccles M. R., Szeto J., McNoe L. A., Yun K., Maw M. A., Smith P. J., Reeve A. E. Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumor. Nature. 362:1993;749-751.
14. KIP2. Am. J. Hum. Genet. 61:1997;295-303.
15. Ping A. J., Reeve A. E., Law D. J., Young M. D., Boehnke M., Feinberg A. P. Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. Am. J. Hum. Genet. 44:1989;720-723.
16. Rainier S., Johnson L. A., Dobry C. J., Ping A. J., Grundy P. E., Feinberg A. P. Relaxation of imprinted genes in human cancer. Nature. 362:1993;747-749.
17. Reeve A. E., Sih S. A., Raizis A. M., Feinberg A. P. Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells. Mol. Cell. Biol. 9:1989;1799-1803.
18. Reik W., Howlett S. K., Surani M. A. Imprinting by DNA methylation: From transgenes to endogenous gene sequences. Development (Suppl.). 1990;99-106.
19. Schroeder W. T., Chao L. Y., Dao D. D., Strong L. C., Pathak S., Riccardi V., Lewis W. H., Saunders G. F. Nonrandom loss of maternal chromosome 11 alleles in Wilms' tumors. Am. J. Hum. Genet. 40:1987;413-420.
20. Scrable H., Cavenee W., Ghavimi F., Lovell M., Morgan K., Sapienza C. A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting. Proc. Natl. Acad. Sci. USA. 86:1989;7480-7484.
21. Steenman M. J. C., Rainier S., Dobry C. J., Grundy P., Horon I., Feinberg A. P. Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumor. Nat. Genet. 7:1994;433-439.
22. Surani M. A., Reik W., Allen N. D. Transgenes as molecular probes for genomic imprinting. Trends Genet. 4:1988;159-162.
23. KIP2. Cancer Res. 56:1996;5723-5727.
24. Wang Q., Curran M. E., Splawski I., Burn T. C., Millholland J. M., VanRaay T. J., Shen J., Timothy K. W., Vincent G. M., de Jager T., Schwartz P. J., Toubin J. A., Moss A. J., Atkinson D. L., Landes G. M., Connors T. D., Keating M. T. Positional cloning of a novel potassium channel gene: KVlqt1 mutations cause cardiac arrhythmias. Nature Genet. 12:1996;17-23.
25. Weitzel J. N., Patel J., Smith D. M., Goodman A., Safaii H., Ball H. G. Molecular genetic changes associated with ovarian cancer. Gyn. Oncol. 55:1994;245-252.
26. Weksberg R., Shen D. R., Fei Y. L., Song Q. L., Squire J. Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome. Nat. Genet. 5:1993;143-150.
27. Winqvist R., Hampton G. M., Mannermaa A., Blanco G., Alavaikko M., Kiviniemi H., Taskinen P. J., Evans G. A., Wright F. A., Newsham I., Cavenee W. K. Loss of heterozygosity for chromosome 11 in primary human breast tumors is associated with poor survival after metastasis. Cancer Res. 55:1995;2660-2664.