Hines J C, Ray D S
Molecular Biology Institute, University of California, Los Angeles 90095-1570, USA.
Mol Biochem Parasitol. 1997 Oct;89(1):41-9. doi: 10.1016/s0166-6851(97)00099-6.
Crithidia fasciculata proteins p18 and p17 are associated with kinetoplast DNA and are encoded by genes KAP2 and KAP3, respectively. Polymerase chain reaction (PCR) amplification using primers within the coding sequences of each gene revealed that the KAP2 and KAP3 genes are linked on the same chromosomal DNA and are separated by a 1.8 kb intergenic region containing several long homopolymer tracts. The KAP2 gene has a 3'UTR of more than 1.1 kb or almost three times as long as the KAP2 coding sequence. Several restriction enzyme polymorphisms in this region of the chromosome are the result of sequence differences between the two alleles of the KAP2 gene. The predicted amino-acid sequences of alleles KAP2-1 and KAP2-2 differ by three non-conservative amino acid substitutions in the highly basic carboxyl tail of the protein and suggest that the protein products could have different physical and biological properties. The KAP2 and KAP3 genes have different patterns of mRNA expression during the cell cycle with the KAP3 transcript varying periodically during the cell cycle in the same manner as transcripts of several kinetoplast and nuclear DNA replication genes.
纤细无鞭毛体蛋白p18和p17与动质体DNA相关,分别由KAP2和KAP3基因编码。使用每个基因编码序列内的引物进行聚合酶链反应(PCR)扩增,结果显示KAP2和KAP3基因位于同一染色体DNA上,且被一个含有多个长同聚物序列的1.8 kb基因间隔区隔开。KAP2基因有一个超过1.1 kb的3'非翻译区,长度几乎是KAP2编码序列的三倍。该染色体区域的几种限制性内切酶多态性是KAP2基因两个等位基因之间序列差异的结果。等位基因KAP2-1和KAP2-2的预测氨基酸序列在蛋白质高度碱性的羧基末端有三个非保守氨基酸取代,这表明蛋白质产物可能具有不同的物理和生物学特性。KAP2和KAP3基因在细胞周期中有不同的mRNA表达模式,KAP3转录本在细胞周期中周期性变化,其变化方式与几种动质体和核DNA复制基因的转录本相同。