Goldman N D, Liu T, Lei K J
J Biol Chem. 1987 May 25;262(15):7001-5.
The gene for human C-reactive protein (CRP) is mapped within a 34-kilobase pair genomic DNA segment identified by chromosome walking through overlapping DNA fragments cloned into a lambda phage library. Within 16 kilobase pairs upstream and downstream of the locus for the authentic CRP gene, only one other sequence homologous to that for CRP could be found. Sequencing analysis indicates this sequence to be a pseudogene with 50-80% region-specific homology. Comparison of the authentic CRP gene cloned from genomic DNA libraries independently prepared from three patients indicates no difference in the 5' and 3' flanking region, promoter region, or coding sequence. Only a polymorphism in the length of the poly(GT) stretch located in the intron is observed. There appears to be only one gene locus and copy per haploid chromosome for the authentic CRP gene and its pseudogene.
人类C反应蛋白(CRP)基因定位在一个34千碱基对的基因组DNA片段内,该片段是通过对克隆到λ噬菌体文库中的重叠DNA片段进行染色体步移鉴定出来的。在真实CRP基因位点上游和下游的16千碱基对内,仅发现了另一个与CRP序列同源的序列。测序分析表明,该序列是一个假基因,具有50 - 80%的区域特异性同源性。对从三名患者独立制备的基因组DNA文库中克隆的真实CRP基因进行比较,结果显示5'和3'侧翼区域、启动子区域或编码序列没有差异。仅观察到位于内含子中的聚(GT)序列长度存在多态性。真实CRP基因及其假基因在每个单倍体染色体上似乎只有一个基因位点和一个拷贝。