Mareni C, Stella A, Origone P, Susca F, Montera M P, Lonoce A, Ponz de Leon M, Sassatelli R, Gentile M, Straface A
Department of Internal Medicine, University of Genova, Italy.
Hum Genet. 1993 Jan;90(5):545-50. doi: 10.1007/BF00217456.
Linkage analysis was performed on 188 subjects belonging to 18 Italian families segregating for familial adenomatous polyposis (FAP) using 7 polymorphic markers (5 restriction fragment length and 2 dinucleotide repeat polymorphisms) mapping in 5q21. A two-point linkage analysis performed with the LINKAGE program gave significant lod scores (> 3) between the Pi227, C11p11, YN5.64, YN5.48 probes and the disease, whereas the ECB27, CB83 and EF5.44 markers showed lower lod scores. Some 11 recombination events were identified from the analysis of 101 meioses. The best map that we could determine confirmed that reported in previous studies. The location of the new marker, CB83, lying between YN5.64 and YN5.48, remains imprecise. No genetic heterogeneity was detected, with all the families showing linkage for at least one of the probes. One 34-year-old individual having an affected haplotype was however classified as healthy after clinical examinations. The results confirm the applicability of the linkage approach for presymptomatic diagnosis of FAP.
对来自18个意大利家族的188名患有家族性腺瘤性息肉病(FAP)的受试者进行了连锁分析,使用了位于5q21的7个多态性标记(5个限制性片段长度多态性和2个二核苷酸重复多态性)。使用LINKAGE程序进行的两点连锁分析显示,Pi227、C11p11、YN5.64、YN5.48探针与疾病之间的对数优势分数(lod scores)显著(>3),而ECB27、CB83和EF5.44标记显示的lod分数较低。通过对101个减数分裂的分析确定了约11个重组事件。我们能够确定的最佳图谱证实了先前研究中报道的结果。新标记CB83位于YN5.64和YN5.48之间,其位置仍不精确。未检测到遗传异质性,所有家族至少对一种探针显示连锁。然而,一名携带患病单倍型的34岁个体在临床检查后被归类为健康。结果证实了连锁分析方法在FAP症状前诊断中的适用性。