Genetic diversification of chemokine CXCL16 and its receptor CXCR6 in primates

被引:4
|
作者
Xu, Feifei [1 ,2 ]
He, Dan [1 ,2 ]
Liu, Jiabin [3 ]
Ni, Qingyong [1 ,2 ]
Lyu, Yongqing [4 ]
Xiong, Shiqiu [5 ]
Li, Yan [1 ,2 ]
机构
[1] Sichuan Agr Univ, Coll Anim Sci & Technol, Wenjiang, Peoples R China
[2] Sichuan Agr Univ, Farm Anim Genet Resources Explorat & Innovat Key, Wenjiang, Peoples R China
[3] Chengdu Res Base Giant Panda Breeding, Sichuan Key Lab Conservat Biol Endangered Wildlif, Chengdu, Sichuan, Peoples R China
[4] Kunming Calmette Int Hosp, Hosp 1, Kunming, Yunnan, Peoples R China
[5] Univ Leicester, Canc Res Ctr, Leicester, Leics, England
关键词
Diversification; CXCL16; CXCR6; Hominoids; Cercopithecoids; MEMBRANE-BOUND CHEMOKINE; AMINO-ACID SITES; FUNCTIONAL DIVERGENCE; MAXIMUM-LIKELIHOOD; EXPRESSION CLONING; SCAVENGER RECEPTOR; CANCER CELLS; TNF-ALPHA; T-CELLS; PROTEIN;
D O I
10.1016/j.dci.2018.04.005
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Chemokine CXCL16 and its receptor CXCR6 are associated with a series of physiological and pathological processes in cooperative and stand-alone fashions. To shed insight into their versatile nature, we studied genetic variations of CXCL16 and CXCR6 in primates. Evolutionary analyses revealed that these genes underwent a similar evolutionary fate. Both genes experienced adaptive diversification with the phylogenetic division of cercopithecoids (Old World monkeys) and hominoids (humans, great apes, and gibbons) from their common ancestor. In contrast, they were conserved in the periods preceding and following the dividing process. In terms of the adaptive diversification between cercopithecoids and hominoids, the adaptive genetic changes have occurred in the mucin-like and chemokine domains of CXCL16 and the N-terminus and transmembrane helixes of CXCR6. In combination with currently available structural and functional information for CXCL16 and CXCR6, the parallels between the evolutionary footprints and the co-occurrence of adaptive diversification at some evolutionary stage suggest that interplay could exist between the diversification-related amino acid sites, or between the domains on which the identified sites are located, in physiological processes such as chemotaxis and/or cell adhesion. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:86 / 94
页数:9
相关论文
共 50 条
  • [31] Role for CXCR6 and its ligand CXCL16 in the pathogenesis of T-cell alveolitis in sarcoidosis
    Agostini, C
    Cabrelle, A
    Calabrese, F
    Bortoli, M
    Scquizzato, E
    Carraro, S
    Miorin, M
    Beghè, B
    Trentin, L
    Zambello, R
    Facco, M
    Semenzato, G
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2005, 172 (10) : 1290 - 1298
  • [32] CXCR6/CXCL16 is required for optimal NKT cell and dendritic cell interactions
    Veinotte, Linnea Lora
    Johnston, Brent
    JOURNAL OF IMMUNOLOGY, 2009, 182
  • [33] Expression analysis and clinical significance of CXCL16/CXCR6 in patients with bladder cancer
    Lee, Jun Taik
    Lee, Sang Don
    Lee, Jeong Zoo
    Chung, Moon Kee
    Ha, Hong Koo
    ONCOLOGY LETTERS, 2013, 5 (01) : 229 - 235
  • [34] ACTIVATION OF CXCL16/CXCR6 PATHWAY BY INFLAMMATION ACCELERATES THE PROGRESSION OF DIABETIC NEPHROPATHY
    Hu, Ze Bo
    Ma, Kun Ling
    Zhang, Yang
    Liu, Liang
    Lu, Jian
    Liu, Bi Cheng
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2016, 31 : 203 - 203
  • [35] The CXCL16/CXCR6 chemokine pathway specifically targets alloreactive T-cells to the bone marrow of mice with leukaemia
    Van der Voort, R.
    Verweij, V.
    Maas, F.
    Vos, J.
    Philippens, M.
    De Witte, T.
    Dolstra, H.
    BONE MARROW TRANSPLANTATION, 2008, 41 : S26 - S26
  • [36] The chemokine CXCL16 induces migration and invasion of glial precursor cells via PI3-kinase-dependent signal transduction of its receptor CXCR6/Bonzo
    Mentlein, Rolf
    Hattermann, Kirsten
    Held-Feindt, Janka
    Ludwig, Andreas
    NEURON GLIA BIOLOGY, 2007, 2 : S134 - S134
  • [37] 趋化因子CXCL16及其受体CXCR6与纤维化
    麻贞贞
    赵金霞
    刘湘源
    中华微生物学和免疫学杂志, 2018, 38 (12) : 943 - 946
  • [38] Down-expression of CXCL16/CXCR6 by hypermethylation involved in pathogenesis of hidradenitis suppurativa
    Wang, Zhongshuai
    Zhao, Huijuan
    Zhai, Wanying
    Zhang, Xiaofeng
    Li, Li
    Yuan, Chen
    Li, Yangqun
    Yan, Yan
    Wang, Baoxi
    EXPERIMENTAL DERMATOLOGY, 2022, 31 : 56 - 56
  • [39] Serum levels of CXCL16 and CXCR6 were elevated in children with primary nephrotic syndrome
    Li Qian
    Sun Shu-zhen
    Zhu Yan-ji
    PEDIATRIC NEPHROLOGY, 2013, 28 (08) : 1587 - 1587
  • [40] ACTIVATION OF CXCL16/CXCR6 PATHWAY BY INFLAMMATION ACCELERATES THE PROGRESSION OF ATHEROSCLEROSIS IN ESRD PATIENTS
    Hu, Ze Bo
    Chen, Yan
    Ma, Kun Ling
    Liu, Bi Cheng
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2016, 31 : 1431 - 1431