Davies W, Harbitz I, Hauge J G
Department of Biochemistry, Norwegian College of Veterinary Medicine, Oslo.
Anim Genet. 1987;18(3):233-40. doi: 10.1111/j.1365-2052.1987.tb00763.x.
A cDNA library for porcine skeletal muscle was established in the vector pBR322. The library was screened with an oligonucleotide probe coding for a hexapeptide from glucosephosphate isomerase (Gpi). A positive clone with an insert of about 450 bp and restriction sites for PstI, BamHI and PvuII was isolated. A 362-bp PstI fragment was sequenced and shown to contain the codons for the hexapeptide as well as the remaining 29 amino acids of this Gpi peptide. The PstI fragment was used to probe pig genomic DNA. The restriction enzymes PvuII and SacI detected a set of polymorphisms with five bands, behaving as a set of insertion/deletion polymorphisms.
构建了一个以pBR322为载体的猪骨骼肌cDNA文库。用编码葡萄糖磷酸异构酶(Gpi)六肽的寡核苷酸探针筛选该文库。分离出一个插入片段约450 bp、具有PstI、BamHI和PvuII酶切位点的阳性克隆。对一个362 bp的PstI片段进行测序,结果表明其包含该六肽的密码子以及该Gpi肽其余的29个氨基酸。用PstI片段探测猪基因组DNA。限制性内切酶PvuII和SacI检测到一组具有五条带的多态性,表现为一组插入/缺失多态性。