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串联重复序列改变犬类 CD1D 基因的结构。

Tandem repeats modify the structure of the canine CD1D gene.

机构信息

Department of Infectious Diseases and Immunology, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 1, 3584 CL, Utrecht, The Netherlands.

出版信息

Anim Genet. 2013 Jun;44(3):352-5. doi: 10.1111/age.12002. Epub 2012 Sep 19.

Abstract

Among the CD1 proteins that present lipid antigens to T cells, CD1d is the only one that stimulates a population of T cells with an invariant T-cell receptor known as NKT cells. Sequencing of a 722 nucleotide gap in the dog (Canis lupus familiaris) genome revealed that the canine CD1D gene lacks a sequence homologous to exon 2 of human CD1D, coding for the start codon and signal peptide. Also, the canine CD1D gene contains three different short tandem repeats that disrupt the expected gene structure. Because canine CD1D cDNA lacks sequences homologous to human exon 2 and 3, the functionality of canine CD1d protein may be affected, and this could have consequences for the development and activation of canine NKT cells.

摘要

在呈现脂质抗原给 T 细胞的 CD1 蛋白中,CD1d 是唯一能够刺激具有不变 T 细胞受体(称为 NKT 细胞)的 T 细胞群体的蛋白。对狗(Canis lupus familiaris)基因组中 722 个核苷酸缺口的测序表明,犬 CD1D 基因缺乏与人 CD1D 外显子 2 同源的序列,该序列编码起始密码子和信号肽。此外,犬 CD1D 基因包含三个不同的短串联重复序列,破坏了预期的基因结构。由于犬 CD1D cDNA 缺乏与人外显子 2 和 3 同源的序列,犬 CD1d 蛋白的功能可能受到影响,这可能对犬 NKT 细胞的发育和激活产生影响。

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