Kunihiro Sumiko, Kawanishi Yuichi, Sano Motoaki, Naito Kimitoshi, Matsuura Yukio, Tateno Yoshio, Gojobori Takashi, Yamagata Youhei, Abe Keietsu, Machida Masayuki
Institute of Molecular and Cell Biology, National Institute of Advanced Industrial Science and Technology, Central 6, 1-1, Higashi, Tsukuba, Ibaraki 305-8566, Japan.
Gene. 2002 May 1;289(1-2):177-84. doi: 10.1016/s0378-1119(02)00547-4.
We have developed a novel method for cloning gene family members by using a polymerase chain reaction technique. The method is based on the amplification of a broad range of homologous genes in combination with the specific inhibition of already cloned genes. To accomplish this, we designed degenerate primers to highly conserved regions among the gene family members, and inhibitory primers to the divergent region at the 3'-margin of each degenerate primer. The 5'-end of the inhibitory primer, the 3'-end of which was aminated, had 3-4 bases overlapping the 3'-end of the degenerate primer. The potential of this method was demonstrated by the successful cloning of a novel member of the yeast MKC7/YAP3 gene family homologue from a filamentous fungus, Aspergillus oryzae, by inhibiting amplification of an already cloned homologue, opsB.
我们开发了一种利用聚合酶链反应技术克隆基因家族成员的新方法。该方法基于广泛扩增同源基因并结合对已克隆基因的特异性抑制。为此,我们针对基因家族成员中的高度保守区域设计了简并引物,并针对每个简并引物3'端的差异区域设计了抑制性引物。抑制性引物的5'端(其3'端进行了胺化修饰)与简并引物的3'端有3 - 4个碱基重叠。通过抑制已克隆的同源基因opsB的扩增,从丝状真菌米曲霉中成功克隆出酵母MKC7/YAP3基因家族同源物的一个新成员,证明了该方法的潜力。