GENETIC MECHANISM ACCOUNTING FOR PRECISE IMMUNOGLOBULIN DOMAIN DELETION IN A VARIANT OF MPC 11 MYELOMA CELLS

被引:25
作者
KENTER, AL
BIRSHTEIN, BK
机构
[1] Department of Cell Biology, Albert Einstein College of Medicine, Bronx
关键词
D O I
10.1126/science.117550
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A variant of the MPC 11 cell line, M 311, produces a short immunoglobulin heavy chain. When compared with the parental γ2b heavy chain, M 311 was found to have a carboxyl terminal deletion comprising the C H3 domain. The COOH-terminal cyanogen bromide (CNBr) cleavage fragment of M 311 is identical to a corresponding segment of a parental heavy chain CNBr fragment, with the exception of a substitution of asparagine for lysine at the COOH-terminal residue. This observation enabled prediction of both the parental DNA sequence in this region and the genetic mechanism which generated the variant, a frameshift followed by premature termination. This hypothesis is supported by studies of the DNA sequence of the MPC 11 γ2b constant region gene. Copyright © 1979 AAAS.
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页码:1307 / 1309
页数:3
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