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果蝇节段极性基因豪猪的人类同源基因MG61/PORC基因的分子克隆及初步特性分析

Molecular cloning and initial characterization of the MG61/PORC gene, the human homologue of the Drosophila segment polarity gene Porcupine.

作者信息

Caricasole Andrea, Ferraro Teresa, Rimland Joseph M, Terstappen Georg C

机构信息

GlaxoSmithKline, Medicines Research Centre, Via Fleming 4, 37135 Verona, Italy.

出版信息

Gene. 2002 Apr 17;288(1-2):147-57. doi: 10.1016/s0378-1119(02)00467-5.

Abstract

Insect and vertebrate Porcupine genes encode multi-pass endoplasmic reticulum proteins involved in the processing of Wnt (wingless and int homologue) proteins, a class of secreted glycoprotein factors homologous to the Drosophila melanogaster segment polarity gene Wingless (Wg). Here we report the cloning of cDNAs encoding the human homologue of the Drosophila gene Porcupine (Porc), the characterization of its genomic structure and the quantitative analysis of its expression in a comprehensive panel of human tissues. The human Porcupine locus (MG61/PORC) spans 15 exons over approximately 12 kb of genomic sequence on Xp11.23. Real-time quantitative expression analysis reveals that MG61/PORC transcripts are expressed in multiple tissues, but are particularly abundant in the brain. Like its mouse and Xenopus homologues, MG61/PORC encodes four protein isoforms (A-D) generated through alternative splicing and expressed in a tissue-specific fashion. Finally, we present evidence indicating that MG61/PORC can influence the activity of a human Wnt7A expression construct in a T-cell factor-responsive reporter assay.

摘要

昆虫和脊椎动物的豪猪基因编码参与Wnt(无翅和int同源物)蛋白加工的多次跨膜内质网蛋白,Wnt蛋白是一类与果蝇黑腹果蝇节段极性基因无翅(Wg)同源的分泌糖蛋白因子。在此,我们报告了编码果蝇基因豪猪(Porc)人类同源物的cDNA的克隆、其基因组结构的特征以及在一组全面的人类组织中其表达的定量分析。人类豪猪基因座(MG61/PORC)在Xp11.23上约12kb的基因组序列上跨越15个外显子。实时定量表达分析表明,MG61/PORC转录本在多种组织中表达,但在脑中特别丰富。与其小鼠和非洲爪蟾同源物一样,MG61/PORC编码通过可变剪接产生并以组织特异性方式表达的四种蛋白质异构体(A-D)。最后,我们提供的证据表明,在T细胞因子反应性报告基因测定中,MG61/PORC可影响人类Wnt7A表达构建体的活性。

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