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通过BclI限制性片段长度变异证明的CHO细胞aprt突变体中等位基因的缺失。

Loss of alleles in aprt mutants of CHO cells demonstrated by BclI restriction-fragment-length variation.

作者信息

Dewyse P, Bradley W E

机构信息

Institut du Cancer de Montréal, Sherbrooke, Québec, Canada.

出版信息

Somat Cell Mol Genet. 1990 May;16(3):225-30. doi: 10.1007/BF01233358.

Abstract

A BclI restriction-fragment-length variation (RFLV) has been identified 7 kb downstream of the 3' end of the adenine phosphoribosyltransferase (aprt) gene in the Chinese hamster CHO cell line. This RFLV generates 19 kb and 17 kb + 2 kb BclI fragments. Three other cell lines derived from different Chinese hamsters are homozygous for this RFLV. The 17 kb + 2 kb allele was mapped to the Z4 chromosome based upon the absence of this allele in the CHO-derived hemizygote AA8-5, whose functional allele is known to map to chromosome Z7. The class 2 aprt+/-line D416 loses the 19-kb allele after undergoing the high-frequency (HF) deletion event, indicating that the HF deletion event occurs on the Z7 chromosome. On the other hand, deletion events in the class 3 heterozygote D423 (which do not spontaneously occur at HF) resulted in loss of the 17 kb + 2 kb allele. This is consistent with a previously proposed model holding that the two aprt alleles in the CHO cell line have different inherent probabilities of undergoing a large deletion event.

摘要

在中国仓鼠CHO细胞系中,已在腺嘌呤磷酸核糖转移酶(aprt)基因3'端下游7 kb处鉴定出一种BclI限制性片段长度变异(RFLV)。这种RFLV产生19 kb和17 kb + 2 kb的BclI片段。来自不同中国仓鼠的其他三个细胞系对此RFLV呈纯合状态。基于CHO衍生的半合子AA8 - 5中不存在该等位基因,将17 kb + 2 kb等位基因定位到Z4染色体上,已知其功能等位基因定位于Z7染色体。2类aprt+/-系D416在经历高频(HF)缺失事件后失去19 kb等位基因,这表明HF缺失事件发生在Z7染色体上。另一方面,3类杂合子D423中的缺失事件(不会自发地高频发生)导致17 kb + 2 kb等位基因丢失。这与先前提出的模型一致,该模型认为CHO细胞系中的两个aprt等位基因发生大缺失事件的固有概率不同。

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