|
|
Binding and Localization Analysis Between Bovine (Bos taurus) Invariant Chain and the Active Fragment of BoLA Class Ⅱ Molecule β Chain |
CHEN Fang-Fang*,**, YU Feng-Mei*, ZHANG Jun, TAN Yang, LIU Cui-Yan, GUI Ya-Ping |
Anhui Province Laboratory of Zoonosis, College of Animal Science and Technology, Anhui Agricultural University, Hefei 230036, China |
|
|
Abstract Bovine leukocyte antigen (BoLA), also named major histocompatibility complex (MHC), its class Ⅱ molecules and chaperone protein, invariant chain (Ii), plays a key role in the processing and presentation of antigenic peptides. In order to understand the characteristics of binding between BoLAⅡβ chain and Ii, and intracellular localization in this process, in this study, mRNA from blood cells of Huaibei yellow cattle (Bos taurus) was extracted and reverse transcribed into cDNA, the genes of BoLAⅡβ, its fragments and Ii were amplified by PCR and then the corresponding eukaryotic and prokaryotic expression plasmids were constructed, respectively. The proteins were expressed and purified by prokaryotic expression system. The binding between Ii and BoLAⅡβ chain or its fragments was detected by pull-down method and Western blot. The co-localization of Ii with BoLAⅡβ and their fragments in cells was observed by laser confocal microscope. The results showed that the recombinant plasmid containing Ii, BoLAⅡβ, BoLAⅡβ(β1β2) and BoLAⅡβ(TC) genes could be induced and purified. BoLAⅡβ and BoLAⅡβ(β1β2) had the active function of binding Ii, but BoLAⅡβ(TC) did not. Meanwhile, Ii could co-localized with BoLAⅡβ, BoLAⅡβ(β1β2) or BoLAⅡβ(TC) in eukaryotic cells. In conclusion, the β1β2 of BoLAⅡβ was the key domain for its intracellular binding and the both domains β1β2 and TC were the functional domains of co-localization with Ii in cells. This study provides an important experimental basis for further study on the transport and mechanism of BoLA molecule and Ii in immune response.
|
Received: 30 November 2021
|
|
Corresponding Authors:
** Corresponding author, fang7828887@126.com
|
|
|
|
[1] 陈芳芳, 谭红黎, 钱艳红, 等. 2020. 鸡恒定链与Rab7b结合并共定位于晚期内吞体[J]. 畜牧兽医学报, 51(12): 3151-3159.
(Chen F F, Tan H L, Qian Y H, et al.2020. Molecular characteristics of chicken Rab7b in localization and binding invariant chain in late cell endocytosis[J]. Acta Veterinaria et Zootechenica Sinica, 51(12): 3151-3159.)
[2] 陈芳芳,张旭,谭红黎,等. 2019. 鸡恒定链协助抗原肽结合MHCⅡ类分子并进入细胞内吞体[J]. 畜牧兽医学报, 50(2):398-405.
(Chen F F, Zhang Xu, Tan H L, et al.2019. Chicken Ii helps antigen peptide bind MHC classⅡ molecules and enter endosomes[J]. Acta Veterinaria et Zootechnia Ainica, 50(2): 398-405.)
[3] 储稳, 罗兰芳, 吕邑旺, 等. 2016. 应用Pull-down 方法获得鸡B-LB分子中结合恒定链的活性片段[J]. 农业生物技术学报, 24(10): 1474-1481.
(Chu w, Luo L F, Lv Y W, er al.2016. Obtaining active segments in chicken (Gallus gallus) B-LB molecule to bind with invariant chain by pull-down method[J]. Journal of Agricultural Biotechnology, 24(10): 1474-1481.)
[4] Basha G, Omilusik K, Chavez-Steenbock A, et al.2012. A CD74-dependent MHC classⅠ endolysosomal cross-presentation pathway[J]. Nature Immunology, 13(3): 237-245.
[5] Biedrzycka A, Radwan J.2008. Population fragmentation and major histocompatibility complex variation in the spotted suslik, Spermophilus suslicus[J]. Molecular Ecology, 17(22): 4801-4811.
[6] Bremnes B, Madsen T, Gedde-Dah M, et al.1994. An LI and ML motif in the cytoplasmic tail of the MHC-associated invariant chain mediate rapid internalization[J]. Journal of Cell Science, 107(7): 2021-2032.
[7] Chen F F, Pan L, Wu C, et al.2012a. Character of chicken polymorphic MHC classⅡ alleles of three chinese local breeds[J]. Poultry Science, 91(5): 1097-1104.
[8] Chen F F, Meng F T, Pan L, et al.2012b. Boosting immune response with the invariant chain segments via associating to non PBR of MHCⅡ class molecule[J]. BMC Immunology, 13: 55.
[9] Chen F F, Pan L, Zhang J G, et al.2014. Allele-dependent association of chicken MHC classⅠmolecules with the invariant chain[J]. Veterinary Immunology Immunopathology, 160(3-4): 273-280.
[10] Chen F F, Lin H B, Li J C, et al.2017. Grass carp (Ctenopharyngodon idellus) invariant chain of the MHC classⅡ chaperone protein associates with the classⅠ molecule[J]. Fish Shellfish Immunology, 63: 1-8.
[11] Cloutier M, Fortin J S, Thibodeau J, 2021. The transmembrane domain and luminal C-terminal region independently support invariant chain trimerization and assembly with MHCⅡ into nonamers[J]. BMC Immunology, 22(1): 56.
[12] Derakhshani H, Plaizier J C,Buck J D, et al.2018. Association of bovine major histocompatibility complex (BoLA) gene polymorphism with colostrum and milk microbiota of dairy cows during the first week of lactation[J]. Microbiome, 6(1): 203.
[13] Dijkstra J M, Yamaguchi T.2019. Ancient features of the MHC classⅡ presentation pathway, and a model for the possible origin of MHC molecules[J]. Immunogenetics, 71(3): 233-249.
[14] Eizaguirre C, Yeates S E, Lenz T L, et al.2009. MHC-based mate choice combines good genes and maintenance of MHC polymorphism[J]. Molecular Ecology, 18(15): 3316-3329.
[15] Elliott E A, Drake J R, Amigorena S, et al.1994. The invariant chain is required for intracellular transport and function of major histocompatibility complex classⅡ molecules[J]. Journal of Experimental Medicine, 179(2): 681-694.
[16] Esposito I, Cicconi P, D'Alise A M, et al.2020. MHC classⅡ invariant chain-adjuvanted viral vectored vaccines enhances T cell responses in humans[J]. Science Translational Medicine, 12(548): eaaz7715.
[17] Forletti A, Lützelschwab C M, Cepeda R, et al.2020. Early events following bovine leukaemia virus infection in calves with different alleles of the major histocompatibility complex DRB3 gene[J]. Veterinary Research, 13;51(1): 4.
[18] Gelin C, Sloma I, Charron D, et al.2009. Regulation of MHC Ⅱ and CD1 antigen presentation: from ubiquity to security[J]. Journal of Leukocyte Biology, 85(2): 215-224.
[19] Gu X, Nei M.1999. Locus specificity of polymorphic alleles and evolution by a birth-and-death process in mammalian MHC genes[J]. Molecular and Biological Ecology, 16(2): 147-156.
[20] Gunther S, Schlundt A, Sticht J, et al.2010. Bidirectional binding of invariant chain peptides to an MHC classⅡ molecule[J]. Proceedings of the National Academy of Sciences of USA, 107(51): 22219-22224.
[21] Harbour J C, Lyski Z L, Schell J B, et al.2021.Cellular and humoral immune responses in mice immunized with vaccinia virus expressing the SARS-CoV-2 spike protein[J]. Journal of Immunology, 206(11): 2596-2604.
[22] Hughes C R, Miles S, Walbroehl J M.2008. Support for the minimal essential MHC hypothesis: A parrot with a single, highly polymorphic MHC classⅡ B gene[J]. Immunogenetics, 60(5): 219-231.
[23] Kita Y F, Hosomichi K, Kohara S, et al.2009. MHC classⅠ A loci polymorphism and diversity in three Southeast Asian populations of cynomolgus macaque[J]. Immunogenetics, 61(9): 635-648.
[24] Koutsogiannouli E A, Moutou K A, Sarafidou T, et al.2009. Major histocompatibility complex variation at classⅡ DQA locus in the brown hare (Lepus europaeus)[J]. Molecular Ecology, 18(22): 4631-4649.
[25] Lamberth K, Roeder G, Hamdahl M, et al.2008. The peptide-binding specificity of HLA-A*3001 demonstrates membership of the HLA-A3 supertype[J]. Immunogenetics, 60(11): 633-643.
[26] Landsverk O J B, Bakke O, Gregers T F.2009. MHCⅡ and the endocytic pathway: Regulation by invariant chain[J]. Scandinavian Journal of Immunology, 70(3): 184-193.
[27] Landsverk O J, Ottesen A H, Berg-Larsen A, et al.2012. Differential regulation of MHCⅡ and invariant chain expression during maturation of monocyte-derived dendritic cells[J]. Journal of Leukocyte Biology, 91(5): 729-737.
[28] Margiotta A, Frei D M, Sendstad I H, et al.2020. Invariant chain regulates endosomal fusion and maturation through an interaction with the SNARE Vti1b[J]. Journal of Cell Science, 133(19): jcs244624.
[29] Neckermann P, Boilesen D R, Willert T, et al.2021. Design and immunological validation of macaca fascicularis papillomavirus type 3 based vaccine candidates in outbred mice: Basis for future testing of a therapeutic papillomavirus vaccine in NHPs[J] . Frontiers in Immunology, 12: 761214.
[30] Othman E, Muhammad G, Ayman H, et al.2018. Five BoLA-DRB3 genotypes detected in egyptian buffalo infected with Foot and Mouth disease virus serotype O[J]. Journal of Genetic Engineering and Biotechnology, 2(16) :513-518.
[31] Pokorska J, Kułaj D, Dusza M, et al.2018. The influence of BoLA-DRB3 alleles on incidence of clinical mastitis, cystic ovary disease and milk traits in holstein friesian cattle[J]. Molecular Biology Reports, 45(5): 917-923.
[32] Rao X, Costa A I, Vanbaarle D, et al.2009. A comparative study of HLA binding affinity and ligand diversity: Implications for generating immunodominant CD8+ T cell responses[J]. Journal of Immunology, 182(3): 1526-1532.
[33] Roche P A, Cresswell P.2011. Proteolysis of the classⅡ-associated invariant chain generates a peptide binding site in intracellular HLA-DR molecules[J]. Journal of Immunology, 187(3): 1076-1080.
[34] Satta Y, O'hUigin C, Takahata N, et al.1994. Intensity of natural selection at the major histocompatibility complex loci[J]. Proceedings of the National Academy of Sciences of the USA, 91(15): 7184-7188.
[35] Shishido T, Kohyama M, Nakai W, et al.2019. Invariant chain p41 mediates production of soluble MHC classⅡ molecules[J]. Biochemical and Biophysical Research Communications, 509(1): 216-221.
[36] Takeshima S N, Ohno A, Aida Y.2019. Bovine leukemia virus proviral load is more strongly associated with bovine major histocompatibility complex classⅡ DRB3 polymorphism than with DQA1 polymorphism in Holstein cow in Japans[J]. Retrovirology, 16(1): 14.
[37] Takeshima S, Nakai Y, Ohta M., et al.2002. Short communication: Characterization of DRB3 alleles in the MHC of Japanese shorthorn cattle by polymerase chain reaction-sequence-based typing[J]. Journal of Dairy Science, 85(6): 1630-1632.
[38] Tallmadge R L, Campbell J A, Miller D C, et al.2010. Analysis of MHC classⅠ genes across horse MHC haplotypes[J]. Immunogenetics, 62(3): 159-172.
[39] Westerdahl H, Wittzell H, Vonschantz T.2000. Mhc diversity in two passerine birds: No evidence for a minimal essential Mhc[J]. Immunogenetics, 52(1-2): 92-100.
[40] Xu A, van Eijk MJ, Park C, et al.1993. Polymorphism in BoLA-DRB3 exon 2 correlates with resistance to persistent lymphocytosis caused by bovine leukemia virus[J]. Journal of Immunology, 151(12): 6977-6985.
[41] Zhong D L, Yu W Y, Liu Y H, et al.2004. Molecular cloning and expression of two chicken invariant chain is forms produced by alternative splicing[J]. Immunogenetics, 56(9): 650-656. |
[1] |
CHI Zhi-Jiao, Chelmeg, CHENG Gong, SU Ya, CHENG Li-Xin, LIU Jian-Feng, CAO Gui-Fang, BAO Si-Qin, ZAN Lin-Sen, TONG Bin. Association Analysis Between Polymorphisms in FABP4, FASN and TCAP Genes and Growth and Carcass Traits in Qinchuan Cattle (Bos taurus)[J]. 农业生物技术学报, 2022, 30(8): 1488-1498. |
|
|
|
|