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

机译: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基转移酶基因座功能性半合子的基础。

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摘要

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.
机译:CHO-AT3-2中国仓鼠卵巢细胞系在功能上对腺嘌呤磷酸核糖基转移酶(APRT; EC 2.4.2.7)位点是半合子的。可以以高自发频率从野生型CHO细胞群体中分离出1类APRT +/-杂合子,例如CHO-AT3-2。西蒙等。 [Simon,A. E.,Taylor,M. W.,Bradley,W. E. C.&Thompson,L.(1982)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与1类APRT +/-杂合子的自发产生和2类APRT +中APRT-突变体的高频发生有关/-杂合子种群。此事件似乎仅在两个APRT等位基因之一发生。为了调查此高频事件的性质,并确定CHO-AT3-2细胞中APRT基因座功能性半合子性的遗传基础,我们已经通过使用CHO-AT3-2小鼠体细胞杂种来定位了APRT基因座。我们的数据证实,CHO-AT3-2细胞具有位于Z7染色体上的单个功能性APRT等位基因。 CHO-AT3-2的核型分析显示,在应放置其他APRT等位基因的区域中,Z4染色体长臂上存在间隙缺失。为了确定Z4q间质性缺失是否导致APRT基因的物理缺失,分析了丢失或保留Z4q染色体的CHO-AT3-2-小鼠细胞杂种的DNA,以确定CHO APRT编码序列的存在。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位点自发产生功能性半合子的原因。

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