Expression of the Ian family of putative GTPases during T cell development and description of an Ian with three sets of GTP/GDP-binding motifs

被引:26
作者
Dion, C
Carter, C
Hepburn, L
Coadwell, WJ
Morgan, G
Graham, M
Pugh, N
Anderson, G
Butcher, GW [1 ]
Miller, JR
机构
[1] Babraham Inst, Cambridge CB2 4AT, England
[2] Univ Birmingham, Sch Med, Dept Anat, Edgbaston, England
基金
英国生物技术与生命科学研究理事会;
关键词
diabetes; GTPases; lymphopenia; rat; T lymphocytes;
D O I
10.1093/intimm/dxh302
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Reports suggest that two members of the novel immune-associated nucleotide (Ian) GTPase family, Ian1 and Ian5, play roles in T cell development. We performed real-time PCR analysis of the expression of Ian genes of the rat during T cell maturation, in macrophages and in cell lines. We found that all of the genes were expressed at relatively low levels at the early double-negative thymocyte stage but were expressed more strongly at later cell stages. Our study also revealed the fact that the previously reported Ian9, Ian10 and Ian11 genes are, instead, parts of a single gene for which we retain the name Ian9, potentially encoding a GTPase with a highly unusual triplicated structure. Antisera were developed against both Ian1 and Ian9. We established that Ian9 is produced as an similar to 75-kDa protein in both T cells and thymocytes. We observed that levels of both Ian1 and Ian9 proteins are profoundly reduced in T cells from lymphopenic rats as compared with wild-type rats. It was demonstrated that thymocytes and B cells from lymphopenic rats (Ian5 null) did not show enhanced sensitivity to gamma-irradiation-induced apoptosis.
引用
收藏
页码:1257 / 1268
页数:12
相关论文
共 60 条
[11]   Molecular cloning of Ian4:: a BCR/ABL-induced gene that encodes an outer membrane mitochondrial protein with GTP-binding activity [J].
Dahéron, L ;
Zenz, T ;
Siracusa, LD ;
Brenner, C ;
Calabretta, B .
NUCLEIC ACIDS RESEARCH, 2001, 29 (06) :1308-1316
[12]   RAT-X-RAT HYBRID MYELOMAS AND A MONOCLONAL ANTI-FD PORTION OF MOUSE IGG [J].
GALFRE, G ;
MILSTEIN, C ;
WRIGHT, B .
NATURE, 1979, 277 (5692) :131-133
[13]  
GOUT PW, 1980, CANCER RES, V40, P2433
[14]  
Groen H, 1996, J IMMUNOL, V156, P1269
[15]  
Hernández-Hoyos G, 1999, EUR J IMMUNOL, V29, P1832, DOI 10.1002/(SICI)1521-4141(199906)29:06&lt
[16]  
1832::AID-IMMU1832&gt
[17]  
3.0.CO
[18]  
2-F
[19]   The diabetes-prone BB rat carries a frameshift mutation in Ian4, a positional candidate of Iddm1 [J].
Hornum, L ;
Romer, J ;
Markholst, H .
DIABETES, 2002, 51 (06) :1972-1979
[20]  
HOSSEINZADEH H, 1993, J IMMUNOL, V150, P1670