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高频结构基因缺失作为中国仓鼠卵巢细胞中腺嘌呤磷酸核糖转移酶基因座功能半合子状态的基础。

High-frequency structural gene deletion as the basis for functional hemizygosity of the adenine phosphoribosyltransferase locus in Chinese hamster ovary cells.

作者信息

Adair G M, Stallings R L, Nairn R S, Siciliano M J

出版信息

Proc Natl Acad Sci U S A. 1983 Oct;80(19):5961-4. doi: 10.1073/pnas.80.19.5961.

Abstract

The CHO-AT3-2 Chinese hamster ovary cell line is functionally hemizygous for the adenine phosphoribosyltransferase (APRT; EC 2.4.2.7) locus. Class 1 APRT +/- heterozygotes, such as CHO-AT3-2, can be isolated at high spontaneous frequencies from wild-type CHO cell populations. Simon et al. [Simon, A. E., Taylor, M. W., Bradley, W. E. C. & Thompson, L. (1982) Mol. Cell. Biol. 2, 1126-1133] have proposed that a high-frequency event that inactivates one APRT allele might be responsible for both the spontaneous generation of class 1 APRT +/- heterozygotes and the high-frequency occurrence of APRT- mutants in class 2 APRT +/- heterozygote populations. This event appears to occur at only one of the two APRT alleles. To investigate the nature of this high-frequency event, and to determine the genetic basis for functional hemizygosity of the APRT locus in CHO-AT3-2 cells, we have mapped the APRT locus by using CHO-AT3-2-mouse somatic cell hybrids. Our data confirm that CHO-AT3-2 cells have a single functional APRT allele, which is located on the Z7 chromosome. Karyotypic analysis of CHO-AT3-2 revealed an interstitial deletion on the long arm of the Z4 chromosome, in the very region where the other APRT allele should be located. To determine whether the Z4q interstitial deletion had resulted in physical loss of the APRT gene, DNA from CHO-AT3-2-mouse cell hybrids that had either lost or retained the Z4q- chromosome was analyzed for the presence of CHO APRT coding sequences. Our data suggest that allele-specific high-frequency structural gene deletion events involving the long arm of chromosome Z4 are responsible for the spontaneous generation of functional hemizygosity at the APRT locus in CHO cells.

摘要

CHO-AT3-2中国仓鼠卵巢细胞系在腺嘌呤磷酸核糖转移酶(APRT;EC 2.4.2.7)基因座上功能半合子。1类APRT+/-杂合子,如CHO-AT3-2,可以以高自发频率从野生型CHO细胞群体中分离出来。西蒙等人[西蒙,A.E.,泰勒,M.W.,布拉德利,W.E.C.和汤普森,L.(1982年)《分子细胞生物学》2,1126 - 1133]提出,使一个APRT等位基因失活的高频事件可能是1类APRT+/-杂合子的自发产生以及2类APRT+/-杂合子群体中APRT-突变体的高频出现的原因。该事件似乎仅发生在两个APRT等位基因中的一个。为了研究这个高频事件的性质,并确定CHO-AT3-2细胞中APRT基因座功能半合子的遗传基础,我们通过使用CHO-AT3-2-小鼠体细胞杂种对APRT基因座进行了定位。我们的数据证实,CHO-AT3-2细胞有一个单一的功能性APRT等位基因,位于Z7染色体上。对CHO-AT3-2的核型分析显示Z4染色体长臂存在中间缺失,就在另一个APRT等位基因应该所在的区域。为了确定Z4q中间缺失是否导致APRT基因的物理丢失,分析了来自已经丢失或保留Z4q-染色体的CHO-AT3-2-小鼠细胞杂种的DNA中CHO APRT编码序列的存在情况。我们的数据表明,涉及Z4染色体长臂的等位基因特异性高频结构基因缺失事件是CHO细胞中APRT基因座功能半合子自发产生的原因。

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