Quantification of the paternal allele bias for new germline mutations in the retinoblastoma gene

被引:41
作者
Dryja, TP [1 ]
Morrow, JF [1 ]
Rapaport, JM [1 ]
机构
[1] HARVARD UNIV,MASSACHUSETTS EYE & EAR INFIRM,SCH MED,TAYLOR SMITH LAB,BOSTON,MA 02114
关键词
D O I
10.1007/s004390050531
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
New germline mutations in the human retinoblastoma gene are known to arise preferentially on paternally derived chromosomes, but the magnitude of that bias has not been measured. We evaluated 49 cases with a new germline mutation and found that in 40 cases (82%) the mutation arose on the paternally derived allele. We also evaluated 48 cases likely to have a somatic initial mutation; in this group the initial mutation arose on paternal or maternal chromosomes with approximately equal frequency. There was no statistically significant difference in the average age of fathers of children with new paternal germline mutations from the average age of fathers of children with new maternal germline mutations or somatic initial mutations. Combining the data with that from previous reports from other groups. the proportion of new germline mutations arising on a paternally derived allele is 85% (based on 72 cases; 95% confidence interval 76-93%). This number can be useful in the genetic counseling of some families with retinoblastoma.
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收藏
页码:446 / 449
页数:4
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