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GPR99,一种与核苷酸受体新亚组具有同源性的新型G蛋白偶联受体。

GPR99, a new G protein-coupled receptor with homology to a new subgroup of nucleotide receptors.

作者信息

Wittenberger Timo, Hellebrand Susanne, Munck Antonia, Kreienkamp Hans-Jürgen, Schaller H Chica, Hampe Wolfgang

机构信息

Zentrum für Molekulare Neurobiologie, Universität Hamburg, Martinistr, 52, D-20246 Hamburg, Germany.

出版信息

BMC Genomics. 2002 Jul 5;3:17. doi: 10.1186/1471-2164-3-17.

Abstract

BACKGROUND

Based on sequence similarity, the superfamily of G protein-coupled receptors (GPRs) can be subdivided into several subfamilies, the members of which often share similar ligands. The sequence data provided by the human genome project allows us to identify new GPRs by in silico homology screening, and to predict their ligands.

RESULTS

By searching the human genomic database with known nucleotide receptors we discovered the gene for GPR99, a new orphan GPR. The mRNA of GPR99 was found in kidney and placenta. Phylogenetic analysis groups GPR99 into the P2Y subfamily of GPRs. Based on the phylogenetic tree we propose a new classification of P2Y nucleotide receptors into two subgroups predicting a nucleotide ligand for GPR99. By assaying known nucleotide ligands on heterologously expressed GPR99, we could not identify specifically activating substances, indicating that either they are not agonists of GPR99 or that GPR99 was not expressed at the cell surface. Analysis of the chromosomal localization of all genes of the P2Y subfamily revealed that all members of subgroup "a" are encoded by less than 370 kb on chromosome 3q24, and that the genes of subgroup "b" are clustered on one hand to chromosome 11q13.5 and on the other on chromosome 3q24-25.1 close to the subgroup "a" position. Therefore, the P2Y subfamily is a striking example for local gene amplification.

CONCLUSIONS

We identified a new orphan receptor, GPR99, with homology to the family of G protein-coupled nucleotide receptors. Phylogenetic analysis separates this family into different subgroups predicting a nucleotide ligand for GPR99.

摘要

背景

基于序列相似性,G蛋白偶联受体(GPRs)超家族可细分为几个亚家族,其成员通常共享相似的配体。人类基因组计划提供的序列数据使我们能够通过计算机同源性筛选鉴定新的GPRs,并预测其配体。

结果

通过用已知的核苷酸受体搜索人类基因组数据库,我们发现了GPR99基因,一种新的孤儿GPR。在肾脏和胎盘中发现了GPR99的mRNA。系统发育分析将GPR99归入GPRs的P2Y亚家族。基于系统发育树,我们提出了一种将P2Y核苷酸受体分为两个亚组的新分类方法,预测了GPR99的核苷酸配体。通过检测在异源表达的GPR99上的已知核苷酸配体,我们无法鉴定出特异性激活物质,这表明它们要么不是GPR99的激动剂,要么GPR99未在细胞表面表达。对P2Y亚家族所有基因的染色体定位分析表明,“a”亚组的所有成员在3号染色体q24上由小于370 kb的基因编码,而“b”亚组的基因一方面聚集在11号染色体q13.5上,另一方面聚集在靠近“a”亚组位置的3号染色体q24-25.1上。因此,P2Y亚家族是局部基因扩增的一个显著例子。

结论

我们鉴定了一种新的孤儿受体GPR99,它与G蛋白偶联核苷酸受体家族具有同源性。系统发育分析将该家族分为不同的亚组,预测了GPR99的核苷酸配体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7dfb/117779/2b9dca04ce67/1471-2164-3-17-1.jpg

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