CAJ | 학술논문

从腹股沟淋巴结或血液中提取总RNA，根据人的Fas基因的cDNA序列设计上、下游引物，通过RT-PCR扩增出三种猕猴属动物Fas基因的cDNA片段，将片段克隆到pGEM-T Easy载体中，筛选阳性克隆并进行序列测定。恒河猴Fas基因编码序列为1005 bp，GenBank收录号为AY007572；熊猴的编码序列为996bp，GenBank收录号为AF326208;短尾猴的编码序列为933bp，GenBank收录号为AF332357。对五种已知的灵长类动物的Fas基因进行序列比较，结果表明Fas基因的保守区域具有高度保守性，而处于编码序列中间的一段低复杂度序列在不同的物种间具有很高的变异性。
종복고구림파결혹혈액중제취총RNA，근거인적Fas기인적cDNA서렬설계상、하유인물，통과RT-PCR확증출삼충미후속동물Fas기인적cDNA편단，장편단극륭도pGEM-T Easy재체중，사선양성극륭병진행서렬측정。항하후Fas기인편마서렬위1005 bp，GenBank수록호위AY007572；웅후적편마서렬위996bp，GenBank수록호위AF326208;단미후적편마서렬위933bp，GenBank수록호위AF332357。대오충이지적령장류동물적Fas기인진행서렬비교，결과표명Fas기인적보수구역구유고도보수성，이처우편마서렬중간적일단저복잡도서렬재불동적물충간구유흔고적변이성。
Total RNA were extracted from inguinal lymph nodes o r blood.The Fas cDNA fragments of three macaca species were obtained by RT-P CR using the upper and low primers according to the Fas gene of human,and th en cloned into pGEM-T Easy vector.The positive clones were sequenced.For the fir st time we cloned the Fas genes of Macaca mulatta,Macaca assamensis and Macaca arctoides,the encoding sequences are 1005bp, 996bp and 933bp, respect ively.Finally we compared the sequences of Fas genes among five primate spec ies that have already been submitted to GenBank.The results confirmed the conser vation of regions in two ends of Fas genes,and the high variability of a low complexity region in middle of every Fas gene.