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多发性内分泌腺瘤1型基因定位于11号染色体,在胰岛素瘤中缺失。

Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma.

作者信息

Larsson C, Skogseid B, Oberg K, Nakamura Y, Nordenskjöld M

机构信息

Department of Clinical Genetics, Karolinska Hospital, Stockholm, Sweden.

出版信息

Nature. 1988 Mar 3;332(6159):85-7. doi: 10.1038/332085a0.

Abstract

Multiple endocrine neoplasia type 1 (MEN-1) is a predisposition to hyperplasia of the parathyroid glands, and to hyperplasia or tumours of the anterior pituitary and the endocrine pancreas, and is inherited as an autosomal dominant trait. Here we map the MEN-1 locus to chromosome 11 by family studies, and demonstrate tight linkage with the human muscle phosphorylase gene. By comparing constitutional and tumour tissue genotypes of insulinomas from a pair of brothers who had inherited MEN-1 from their mother, we have shown that oncogenesis in these cases involves unmasking of a recessive mutation at this locus.

摘要

1型多发性内分泌腺瘤病(MEN-1)是一种易患甲状旁腺增生、垂体前叶和内分泌胰腺增生或肿瘤的疾病,呈常染色体显性遗传。我们通过家系研究将MEN-1基因座定位到11号染色体,并证明它与人类肌肉磷酸化酶基因紧密连锁。通过比较一对从母亲那里遗传了MEN-1的兄弟的胰岛素瘤的正常组织和肿瘤组织基因型,我们发现这些病例中的肿瘤发生涉及该基因座隐性突变的暴露。

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