Weiss B, Wolk K, Grünberg B H, Volk H-D, Sterry W, Asadullah K, Sabat R
Enabling Technologies, Schering AG, Berlin, Germany.
Genes Immun. 2004 Aug;5(5):330-6. doi: 10.1038/sj.gene.6364104.
We have identified the mouse and rat homologs of human interleukin-22 receptor alpha 2 (IL-22R alpha 2) and compared the localization, structure, and expression of the encoding murine and human genes. The mouse IL-22R alpha 2-encoding gene is located on chromosome 10A3 between, like in human, the genes for interferon-gamma R1 and IL-20R1. It spans a region of approximately 10 kb therefore being three times shorter than the human gene. Although the overall gene structure in both species is similar, the mouse gene lacks a counterpart to the third coding exon of the human gene known to be alternatively spliced. Like in human, mouse and rat IL-22R alpha 2 exist only as soluble receptors as deduced from the lack of transmembrane and intracellular domains encoding sequences. Quantitative expression analyses showed, analogically to the human system, a limited tissue distribution of mouse IL-22R alpha 2 mRNA. Differential modulation of IL-22R alpha 2 mRNA expression was observed upon systemic inflammation in mice in spleen, thymus, and lymph node.
我们已鉴定出人类白细胞介素-22受体α2(IL-22Rα2)的小鼠和大鼠同源物,并比较了编码小鼠和人类基因的定位、结构及表达。小鼠IL-22Rα2编码基因位于10A3染色体上,与人类一样,在干扰素-γR1和IL-20R1基因之间。它跨越约10 kb的区域,因此比人类基因短三倍。尽管两个物种的整体基因结构相似,但小鼠基因缺少人类基因已知可选择性剪接的第三个编码外显子的对应物。与人类一样,从小鼠和大鼠IL-22Rα2缺乏跨膜和细胞内结构域编码序列推断,它们仅作为可溶性受体存在。定量表达分析表明,与人类系统类似,小鼠IL-22Rα2 mRNA的组织分布有限。在小鼠全身性炎症时,在脾脏、胸腺和淋巴结中观察到IL-22Rα2 mRNA表达的差异调节。