Moghrabi N N, Naylor S L, Van Veldhoven P P, Baumgart E, Dawson D B, Bennett M J
Department of Pathology, University of Texas Southwestern Medical Center at Dallas, USA.
Biochem Biophys Res Commun. 1997 Feb 24;231(3):767-9. doi: 10.1006/bbrc.1997.6192.
PCR and rodent/human somatic cell hybrids were used to localize the human peroxisomal branched-chain acyl-CoA oxidase gene. Oligonucleotide primers were chosen to specifically amplify human hBCox DNA. The amplified sequence contained two restriction enzyme sites which were used to verify the authenticity of the amplified DNA. Initially, the gene was localized to human chromosome 3 by screening genomic DNA from a hybrid mapping panel. Additional hybrids retaining well-characterized fragments of human chromosome 3 were screened to further localize the gene to 3p21.1.p14.2.
采用聚合酶链反应(PCR)和啮齿动物/人类体细胞杂交技术来定位人类过氧化物酶体支链酰基辅酶A氧化酶基因。选择寡核苷酸引物以特异性扩增人类hBCox DNA。扩增序列包含两个限制性酶切位点,用于验证扩增DNA的真实性。最初,通过筛选来自杂交定位板的基因组DNA将该基因定位到人类3号染色体上。对保留有特征明确的人类3号染色体片段的其他杂种细胞进行筛选,以进一步将该基因定位到3p21.1.p14.2。