Preferential retention of paternal alleles in human retinoblastoma: evidence for genomic imprinting.

R. J. Leach; A. N. Magewu; J. D. Buckley; W. F. Benedict; C. Rother; A. L. Murphree; S. Griegel; M. F. Rajewsky; P. A. Jones

Preferential retention of paternal alleles in human retinoblastoma: evidence for genomic imprinting.

R. J. Leach, A. N. Magewu, J. D. Buckley, W. F. Benedict, C. Rother, A. L. Murphree, S. Griegel, M. F. Rajewsky, P. A. Jones

Research output: Contribution to journal › Article › peer-review

27 Scopus citations

Abstract

The origins of the initial mutations in sporadic retinoblastoma were explored using polymorphic markers from chromosome 13q. The paternal chromosome was maintained in 3 of 3 informative bilateral tumors which had undergone reduction to homozygosity for regions of this chromosome. The paternal chromosome was maintained in 7 of 8 informative unilateral tumors which likewise demonstrated a reduction of homozygosity. These data are in contrast to previously published studies of chromosome retention in unilateral retinoblastoma [Dryja, T. P., Mukai, S., Petersen, R., Rapaport, J. M., Walton, D., and Yandel, D. W. Nature (Lond.), 339: 556-558, 1989; Zhu, Z., Dunn, J. M., Phillips, R. A., Goddard, A. D., Paton, K. E., Becker, A., and Gallie, B. L. Nature (Lond.), 340: 312-313, 1989] and provide the first evidence that genomic imprinting may play a role in this disease.

Original language	English (US)
Pages (from-to)	401-406
Number of pages	6
Journal	Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research
Volume	1
Issue number	9
State	Published - Sep 1990
Externally published	Yes

ASJC Scopus subject areas

Molecular Biology
Cell Biology

Cite this

Leach, R. J., Magewu, A. N., Buckley, J. D., Benedict, W. F., Rother, C., Murphree, A. L., Griegel, S., Rajewsky, M. F., & Jones, P. A. (1990). Preferential retention of paternal alleles in human retinoblastoma: evidence for genomic imprinting. Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research, 1(9), 401-406.

Preferential retention of paternal alleles in human retinoblastoma : evidence for genomic imprinting. / Leach, R. J.; Magewu, A. N.; Buckley, J. D.; Benedict, W. F.; Rother, C.; Murphree, A. L.; Griegel, S.; Rajewsky, M. F.; Jones, P. A.

In: Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research, Vol. 1, No. 9, 09.1990, p. 401-406.

Research output: Contribution to journal › Article › peer-review

Leach, R. J. ; Magewu, A. N. ; Buckley, J. D. ; Benedict, W. F. ; Rother, C. ; Murphree, A. L. ; Griegel, S. ; Rajewsky, M. F. ; Jones, P. A. / Preferential retention of paternal alleles in human retinoblastoma : evidence for genomic imprinting. In: Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research. 1990 ; Vol. 1, No. 9. pp. 401-406.

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abstract = "The origins of the initial mutations in sporadic retinoblastoma were explored using polymorphic markers from chromosome 13q. The paternal chromosome was maintained in 3 of 3 informative bilateral tumors which had undergone reduction to homozygosity for regions of this chromosome. The paternal chromosome was maintained in 7 of 8 informative unilateral tumors which likewise demonstrated a reduction of homozygosity. These data are in contrast to previously published studies of chromosome retention in unilateral retinoblastoma [Dryja, T. P., Mukai, S., Petersen, R., Rapaport, J. M., Walton, D., and Yandel, D. W. Nature (Lond.), 339: 556-558, 1989; Zhu, Z., Dunn, J. M., Phillips, R. A., Goddard, A. D., Paton, K. E., Becker, A., and Gallie, B. L. Nature (Lond.), 340: 312-313, 1989] and provide the first evidence that genomic imprinting may play a role in this disease.",

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AU - Magewu, A. N.

AU - Buckley, J. D.

AU - Benedict, W. F.

AU - Rother, C.

AU - Murphree, A. L.

AU - Griegel, S.

AU - Rajewsky, M. F.

AU - Jones, P. A.

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AB - The origins of the initial mutations in sporadic retinoblastoma were explored using polymorphic markers from chromosome 13q. The paternal chromosome was maintained in 3 of 3 informative bilateral tumors which had undergone reduction to homozygosity for regions of this chromosome. The paternal chromosome was maintained in 7 of 8 informative unilateral tumors which likewise demonstrated a reduction of homozygosity. These data are in contrast to previously published studies of chromosome retention in unilateral retinoblastoma [Dryja, T. P., Mukai, S., Petersen, R., Rapaport, J. M., Walton, D., and Yandel, D. W. Nature (Lond.), 339: 556-558, 1989; Zhu, Z., Dunn, J. M., Phillips, R. A., Goddard, A. D., Paton, K. E., Becker, A., and Gallie, B. L. Nature (Lond.), 340: 312-313, 1989] and provide the first evidence that genomic imprinting may play a role in this disease.

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Preferential retention of paternal alleles in human retinoblastoma: evidence for genomic imprinting.

Abstract

ASJC Scopus subject areas

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