CHROMOSOMAL LOCATION AND ISOFORM ANALYSIS OF MOUSE FC-EPSILON-RII/CD23

被引:25
作者
CONRAD, DH
KOZAK, CA
VERNACHIO, J
SQUIRE, CM
RAO, M
EICHER, EM
机构
[1] NIAID, MOLEC MICROBIOL LAB, BETHESDA, MD 20892 USA
[2] JACKSON LAB, BAR HARBOR, ME 04609 USA
[3] JOHNS HOPKINS UNIV, DEPT MOLEC BIOL, BALTIMORE, MD 21239 USA
关键词
D O I
10.1016/0161-5890(93)90423-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The gene for the mouse low affinity receptor for IgE (Fc(epsilon)RII, also known as CD23) was mapped on Chromosome (Chr) 8 proximal to Plat. This gene, symbolized Fcer2 (formerly Fce2) resides in a region of Chr 8 with linkage homology with human chromosomes 8 and 19. The mouse Fc(epsilon)RII was examined for the presence of alternate N-terminal forms such as seen in humans. An antisense RNA probe was prepared from the 5' end of the cDNA through the first 660 bp of the cDNA and was used to analyze message from Fc(epsilon)RII+ B cells and B cell hybridomas both before and after treatment with interleukin 4 (IL-4). Using RNase protection analysis, a major 640 bp band corresponding to the full length probe was seen, even after activation of the cells with LPS in the presence of IL-4, which is known to give high expression levels of the Fc(epsilon)RII. This result suggests that the mouse does not produce significant levels of an alternate IL-4 inducible Fc(epsilon)RII, as seen in man, and this may explain the more restricted cell lineage expression of the Fc(epsilon)RII in the mouse.
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页码:27 / 33
页数:7
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