A WILD-TYPE MU-S C-TERMINAL GENE IS EXPRESSED IN BLOOMS SYNDROME CELLS

被引:1
|
作者
OZAWA, T
KONDO, N
KATO, Y
MOTOYOSHI, F
SUZUKI, Y
SHIMOZAWA, N
KASAHARA, K
ORII, T
机构
[1] Department of Pediatrics, Gifu University School of Medicine, Gifu
来源
EUROPEAN JOURNAL OF IMMUNOGENETICS | 1994年 / 21卷 / 02期
关键词
D O I
10.1111/j.1744-313X.1994.tb00184.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Selective IgM deficiency is found commonly in patients with Bloom's syndrome (BS). Serum IgM concentrations were low though serum IgG and IgA concentrations were normal in both patients with BS included in the study. In a previous study the authors showed that selective IgM deficiency in BS is due to an abnormality in the maturation of surface IgM-bearing cells into IgM-secreting cells and a failure of secreted mu (mus) mRNA synthesis. The membrane-bound mu (mum) and mus mRNA are produced from transcripts of a single immunoglobulin mu gene by alternative RNA processing pathways. The control of mus mRNA synthesis depends on the addition of poly(A) to mus C-terminal segment. The study described here demonstrated that there was no mutation or deletion in the sequence including mus C-terminal coding sequence, the RNA splice site (GG/TAAAC) at the 5' end of mus C-terminal segment, and the AATAAA poly(A) signal sequence, and second GT-rich element immediately down-stream of the cleavage site in both patients.
引用
收藏
页码:133 / 139
页数:7
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