Szabó J, Heath B, Hill V M, Jackson C E, Zarbo R J, Mallette L E, Chew S L, Besser G M, Thakker R V, Huff V
Section of Endocrinology, Veterans Affairs Medical Center, Salt Lake City, UT, USA.
Am J Hum Genet. 1995 Apr;56(4):944-50.
The syndrome of hereditary hyperparathyroidism and jaw tumors (HPT-JT) is characterized by inheritance, in an autosomal dominant pattern, of recurrent parathyroid adenomas, fibro-osseous tumors of the mandible and/or maxilla, Wilms tumor, and parathyroid carcinoma. This syndrome is clinically and genetically distinct from other endocrine neoplasia syndromes and appears to result from mutation of an endocrine tumor gene designated "HRPT2." We studied five HPT-JT families (59 persons, 20 affected); using PCR-based markers, we instituted a genomewide linkage search after excluding several candidate genes. Lod scores were calculated at various recombination fractions (theta), penetrance 90%. We mapped HRPT2 to the long arm of chromosome 1 (1q21-q31). The maximal lod score was 6.10 at theta = .0 with marker D1S212, or > 10(6) odds in favor of linkage. In six hereditary Wilms tumor families (96 persons, 29 affected), we found no linkage to 1q markers closely linked with HRPT2 (lod scores -15.6 [D1S191] and -17.8 [D1S196], theta = .001). Nine parathyroid adenomas and one Wilms tumor from nine members of three HPT-JT families were examined for loss of heterozygosity at linked loci. The parathyroid adenomas and Wilms tumor showed no loss of heterozygosity for these DNA markers. Our data establish that HRPT2, an endocrine tumor gene on the long arm of chromosome 1, is responsible for the HPT-JT syndrome but not for the classical hereditary Wilms tumor syndrome.
遗传性甲状旁腺功能亢进症合并颌骨肿瘤综合征(HPT-JT)的特征为常染色体显性遗传,表现为复发性甲状旁腺腺瘤、下颌骨和/或上颌骨的骨纤维性肿瘤、威尔姆斯瘤以及甲状旁腺癌。该综合征在临床和遗传学上与其他内分泌肿瘤综合征不同,似乎是由一种名为“HRPT2”的内分泌肿瘤基因突变所致。我们研究了5个HPT-JT家族(共59人,其中20人患病);通过基于聚合酶链反应(PCR)的标记,在排除几个候选基因后,我们进行了全基因组连锁搜索。在不同的重组率(θ)下计算对数优势分数(Lod scores),外显率为90%。我们将HRPT2基因定位到1号染色体长臂(1q21-q31)。在θ = 0时,标记D1S212处的最大Lod分数为6.10,即连锁的优势比大于10^6。在6个遗传性威尔姆斯瘤家族(共96人,其中29人患病)中,我们未发现与HRPT2紧密连锁的1q标记存在连锁关系(标记D1S191处的Lod分数为-15.6,标记D1S196处的Lod分数为-17.8,θ = 0.001)。对3个HPT-JT家族9名成员的9个甲状旁腺腺瘤和1个威尔姆斯瘤进行了连锁位点杂合性缺失检测。这些甲状旁腺腺瘤和威尔姆斯瘤在这些DNA标记上未显示杂合性缺失。我们的数据表明,位于1号染色体长臂上的内分泌肿瘤基因HRPT2是导致HPT-JT综合征的原因,但不是经典遗传性威尔姆斯瘤综合征的病因。