Localization of the gene for MEN 2A.

Henry Ford Hospital medical journal Pub Date : 1992-01-01
J B Lichter, M Difilippantonio, J Wu, D Miller, D C Ward, P J Goodfellow, K K Kidd
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Abstract

The search for the gene that causes the multiple endocrine neoplasia type 2A (MEN 2A) syndrome is entering a new phase. Genetic linkage studies have localized the gene to the pericentromeric region of chromosome 10. The statistical portion of mapping the gene for MEN 2A is nearly complete and now classical molecular biological/gene mapping techniques will be employed. We have used fluorescence in situ hybridization to estimate the size of the MEN2A region to be about 2 to 5 mb, using some liberal assumptions; at worst the region should contain no more than about 10 mb of non-alphoid DNA. Our mapping panels (meiotic recombinant and radiation reduced hybrid) give consistent orders of markers in this small region. We describe our initial attempts to clone the region using yeast artificial chromosomes.

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men2a基因的定位。
对多发性内分泌肿瘤2A型(MEN 2A)综合征基因的研究正进入一个新的阶段。遗传连锁研究已将该基因定位在10号染色体的中心点周围区域。MEN 2A基因定位的统计部分已接近完成,现在将采用经典的分子生物学/基因定位技术。我们使用荧光原位杂交估计MEN2A区域的大小约为2至5mb,使用一些自由的假设;在最坏的情况下,该区域包含的非阿尔法DNA不应超过10mb。我们的图谱面板(减数分裂重组和辐射减少杂交)在这个小区域给出一致的标记顺序。我们描述了我们使用酵母人工染色体克隆该区域的最初尝试。
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Extracellular Ca2+ sensing in C-cells and parathyroid cells. Proceedings of the Urban Health Care Symposium II. June 2-4, 1991. Characterization of the clinical features of five families with hereditary primary cutaneous lichen amyloidosis and multiple endocrine neoplasia type 2. Unusual features of multiple endocrine neoplasia. Long-term follow-up in four large MEN 2 families in The Netherlands.
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