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外周血T细胞表达的三个新的牛T细胞受体δ可变基因亚组的鉴定。

Identification of three new bovine T-cell receptor delta variable gene subgroups expressed by peripheral blood T cells.

作者信息

Herzig Carolyn T A, Blumerman Seth L, Baldwin Cynthia L

机构信息

Department of Veterinary and Animal Sciences, Paige Laboratory, University of Massachusetts, Amherst, MA 01003, USA.

出版信息

Immunogenetics. 2006 Sep;58(9):746-57. doi: 10.1007/s00251-006-0136-z. Epub 2006 Aug 1.

Abstract

To understand the biology of gammadelta T cells in ruminants, it is necessary to have a comprehensive picture of gammadelta T-cell receptor gene diversity and expression. In this study, three new subgroups of bovine T-cell receptor delta (TRD) variable genes were identified by RT-PCR and sequencing and homology with TRDV genes from other mammals determined. Previously unidentified TRDV subgroup genes described in this study include the bovine homologues of ovine TRDV2, TRDV3, and TRDV4 which were named accordingly. TRDV2 subgroup has two genes (TRDV2-1 and TRDV2-2) while we found the previously identified TRDV1 has at least eight genes corresponding to separate genomic sequences. Nucleotide and amino acid sequences for particular gene subgroups between cattle and sheep were more than 87% identical but identities among TRDV subgroups within a species were much less, with bovine TRDV4 having <45% identity to the other three bovine TRDV gene subgroups. Analysis of circulating bovine gammadelta T cells revealed that genes from all four TRDV subgroups were expressed in combination with TRDJ1, TRDJ3, and TRDC, although TRDV4 was the least represented, and all displayed a variety of CDR3 junctional lengths. Finally, some genes within the TRDV1, TRDV2, and TRDV3 subgroups recombined with TRAV incorporating TRAJs, suggesting dual use.

摘要

为了解反刍动物γδ T细胞的生物学特性,有必要全面了解γδ T细胞受体基因的多样性和表达情况。在本研究中,通过逆转录聚合酶链反应(RT-PCR)和测序鉴定了牛T细胞受体δ(TRD)可变基因的三个新亚组,并确定了它们与其他哺乳动物TRDV基因的同源性。本研究中描述的先前未鉴定的TRDV亚组基因包括绵羊TRDV2、TRDV3和TRDV4的牛同源物,并据此命名。TRDV2亚组有两个基因(TRDV2-1和TRDV2-2),而我们发现先前鉴定的TRDV1至少有八个对应于不同基因组序列的基因。牛和绵羊特定基因亚组的核苷酸和氨基酸序列同一性超过87%,但同一物种内TRDV亚组之间的同一性要低得多,牛TRDV4与其他三个牛TRDV基因亚组的同一性小于45%。对循环牛γδ T细胞的分析表明,所有四个TRDV亚组的基因都与TRDJ1、TRDJ3和TRDC结合表达,尽管TRDV4的表达量最少,并且所有基因都显示出多种互补决定区3(CDR3)连接长度。最后,TRDV1、TRDV2和TRDV3亚组中的一些基因与TRAV重组并结合TRAJs,表明存在双重用途。

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