TY - JOUR
T1 - Post-transcriptional allelic exclusion of two functionally rearranged T cell receptor α genes
AU - Furutani, Makoto
AU - Yanagi, Yusuke
AU - Fujisawa, Isao
AU - Nakayama, Toshinori
AU - Kishimoto, Hidehiro
AU - Kulda, Kelsuke
AU - Asano, Yoshihiro
AU - Tada, Tomio
N1 - Funding Information:
The authors are grateful to Drs Ralph T. Kubo, Klaus Rajewsky, Masaru Taniguchi, Aikichi Iwamoto, Tak W Mak and Zottan Ovary for their technical guidance and critical discussion, and to Ms Yoko Yamaguchi and Ms Yunko Morooka for their excellent secretarial assistance. This work was supported by grants from the Ministry of Education, Science and Culture and from Agency for Science and Technology, Japan
PY - 1989/7
Y1 - 1989/7
N2 - We cloned and sequenced T cell receptor (TCR) α and β chain cDNA from a λgt10 library obtained from a murine I-Ak autoreactive helper T cell clone MS202. Two types of cDNA clones for the α chain and one for the β chain were obtained. The two α chain transcripts used two different Vα genes: Vα 4, joined to Jα 11.2; and Vα 5, joined to JαTA13. The four Vα4 cDNA clones obtained did not have a complete sequence, lacking the leader portion. The Vα4 genomic gene segment of MS202 was revealed to contain two exons corresponding to the Vα4.MD13 cDNA sequence, and the potential RNA splicing signals between the two exons were Intact. Both of the a chain cDNA clones showed In-frame rearrangements. Immunoprecipitation of 125I-surfacelabeled lysate of MS202 with anti-TCR antiserum and subsequent electrophonetic analyses indicated that only one of the α chain polypeptides was expressed on the cell surface. Thus, allelic exclusion of the α chain in MS202 is achieved by post-transcriptional regulation rather than rearrangements.
AB - We cloned and sequenced T cell receptor (TCR) α and β chain cDNA from a λgt10 library obtained from a murine I-Ak autoreactive helper T cell clone MS202. Two types of cDNA clones for the α chain and one for the β chain were obtained. The two α chain transcripts used two different Vα genes: Vα 4, joined to Jα 11.2; and Vα 5, joined to JαTA13. The four Vα4 cDNA clones obtained did not have a complete sequence, lacking the leader portion. The Vα4 genomic gene segment of MS202 was revealed to contain two exons corresponding to the Vα4.MD13 cDNA sequence, and the potential RNA splicing signals between the two exons were Intact. Both of the a chain cDNA clones showed In-frame rearrangements. Immunoprecipitation of 125I-surfacelabeled lysate of MS202 with anti-TCR antiserum and subsequent electrophonetic analyses indicated that only one of the α chain polypeptides was expressed on the cell surface. Thus, allelic exclusion of the α chain in MS202 is achieved by post-transcriptional regulation rather than rearrangements.
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U2 - 10.1093/intimm/1.3.281
DO - 10.1093/intimm/1.3.281
M3 - Article
C2 - 2562159
AN - SCOPUS:0024451720
SN - 0953-8178
VL - 1
SP - 281
EP - 288
JO - International immunology
JF - International immunology
IS - 3
ER -