Padgett R A, Wahl G M, Stark G R
Mol Cell Biol. 1982 Mar;2(3):293-301. doi: 10.1128/mcb.2.3.293-301.1982.
Two adjacent fragments of genomic DNA spanning the gene for CAD, which encodes the first three enzymes of UMP biosynthesis, were cloned from a mutant Syrian hamster cell line containing multiple copies of this gene. The mutant was selected for resistance to N-(phosphonacetyl)-L-aspartate, a potent and specific inhibitor of aspartate transcarbamylase, the second enzyme in the pathway. The sizes and positions of about 37 intervening sequences within the 25-kilobase CAD gene were mapped by electron microscopy, and the locations of the 5' and 3' ends of the 7.9-kilobase CAD mRNA were established by electron microscopy and by other hybridization methods. The coding sequences are small (100 to 400 bases), as are most of the intervening sequences (50 to 300 bases). However, there are also several large intervening sequences of up to 5,000 bases each. Two small cytoplasmic polyadenylated RNAs are transcribed from a region just beyond the 5' end of the CAD gene, and their abundance reflects the degree of gene amplification.
从一个含有CAD基因多个拷贝的叙利亚仓鼠突变细胞系中克隆出了两段相邻的基因组DNA片段,该基因编码UMP生物合成途径中的前三种酶。该突变体是通过对N-(膦酰乙酰基)-L-天冬氨酸产生抗性而筛选出来的,N-(膦酰乙酰基)-L-天冬氨酸是该途径中第二种酶——天冬氨酸转氨甲酰酶的一种有效且特异性的抑制剂。通过电子显微镜对25千碱基的CAD基因内约37个间隔序列的大小和位置进行了定位,并通过电子显微镜和其他杂交方法确定了7.9千碱基CAD mRNA的5'端和3'端的位置。编码序列很短(100至400个碱基),大多数间隔序列也是如此(50至300个碱基)。然而,也有几个长达5,000个碱基的大间隔序列。从CAD基因5'端稍远处的一个区域转录出两种小的细胞质多聚腺苷酸化RNA,它们的丰度反映了基因扩增的程度。