Rossi D L, Hardiman G, Copeland N G, Gilbert D J, Jenkins N, Zlotnik A, Bazan J F
Department of Immunobiology, DNAX Research Institute, Palo Alto, California 94304-1104, USA.
Genomics. 1998 Jan 15;47(2):163-70. doi: 10.1006/geno.1997.5058.
We report here the identification and characterization of the mouse homologue of a human CX3C chemokine described by F. Bazan et al. (1997, Nature 385, 640-644). Termed fractalkine, this molecule constitutes a fourth or delta chemokine structural type that displays a novel CX3C sequence fingerprint. Distinct from the alpha, beta, or gamma chemokine families, the polypeptide chain of CX3C predicts a 373-amino-acid type I transmembrane glycoprotein with the chemokine domain resting on top of an extended mucin-like stalk. Comparison of the mouse and human protein chains shows a high degree of conservation in all the globular segments with the exception of the stalk portion. The striking identity of an amino acid stretch encompassing a putative juxtamembrane cleavage site suggests the evolutionary conservation of both membrane-bound and processed CX3C forms. Northern analysis reveals the presence of mouse CX3C mRNA in heart, brain, lung, kidney, skeletal muscle, and testis tissues. The mouse CX3C gene was further localized to the central region of chromosome 8 by interspecific backcross mapping; a related locus was detected on chromosome 11. The novel location of this gene from other chemokine gene clusters adds to the notion that CX3C is a fundamentally new class of chemokine.
我们在此报告由F.巴赞等人(1997年,《自然》385卷,640 - 644页)描述的一种人类CX3C趋化因子的小鼠同源物的鉴定与特性。这种分子被称为fractalkine,它构成了第四种或δ趋化因子结构类型,显示出一种新的CX3C序列指纹。与α、β或γ趋化因子家族不同,CX3C的多肽链预测为一种373个氨基酸的I型跨膜糖蛋白,趋化因子结构域位于一个延伸的粘蛋白样茎的顶部。小鼠和人类蛋白质链的比较显示,除茎部外,所有球状部分都有高度的保守性。包含一个假定的近膜裂解位点的一段氨基酸序列的显著一致性表明膜结合型和加工型CX3C形式在进化上的保守性。Northern分析揭示了小鼠CX3C mRNA在心脏、大脑、肺、肾脏、骨骼肌和睾丸组织中的存在。通过种间回交定位,小鼠CX3C基因进一步定位于8号染色体的中央区域;在11号染色体上检测到一个相关位点。该基因在其他趋化因子基因簇中的新位置进一步证明CX3C是一类全新的趋化因子。