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位于9号染色体p13区域的人类白细胞介素-11受体α链基因IL11RA的分子克隆与特性分析

Molecular cloning and characterization of the human interleukin-11 receptor alpha-chain gene, IL11RA, located on chromosome 9p13.

作者信息

Van Leuven F, Stas L, Hilliker C, Miyake Y, Bilinski P, Gossler A

机构信息

Department of Human Genetics, Katholieke Universiteit Leuven, Belgium.

出版信息

Genomics. 1996 Jan 1;31(1):65-70. doi: 10.1006/geno.1996.0010.

Abstract

The human gene coding for the interleukin-11 receptor (IL11RA) was cloned and its structure analyzed. The gene is composed of 13 exons comprising nearly 10 kb of DNA that was completely sequenced. The intron-exon boundaries were determined based on the mouse Etl2 and interleukin-11 receptor cDNAs that were recently cloned. The protein sequence predicted by the human gene was over 83% identical with its murine counterpart, with very strict conservation of functionally important domains and signatures. Fluorescence in situ hybridization showed the gene to be located on human chromosome 9p13, syntenic with the mouse etl2 gene on chromosome 4. The coding exons of the Interleukin-11 gene were sequenced in a patient with the cartilage-hair hypoplasia syndrome, which has been linked to a gene on chromosome 9, but no functional mutations were detected.

摘要

编码白细胞介素-11受体(IL11RA)的人类基因被克隆并对其结构进行了分析。该基因由13个外显子组成,包含近10 kb的DNA,已对其进行了全序列测定。基于最近克隆的小鼠Etl2和白细胞介素-11受体cDNA确定了内含子-外显子边界。人类基因预测的蛋白质序列与其小鼠对应物的同源性超过83%,功能重要结构域和特征高度保守。荧光原位杂交显示该基因位于人类9号染色体p13上,与小鼠4号染色体上的etl2基因同线。在一名患有软骨毛发发育不全综合征的患者中对白细胞介素-11基因的编码外显子进行了测序,该综合征与9号染色体上的一个基因相关,但未检测到功能突变。

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