Wydner K S, Kim Y, Csiszar K, Boyd C D, Passmore H C
Department of Biological Sciences, Rutgers University, Piscataway, New Jersey 08855-1059, USA.
Genomics. 1997 Mar 1;40(2):342-5. doi: 10.1006/geno.1996.4574.
An intron capture strategy involving use of polymerase chain reaction was used to identify and map the mouse homologue of a human lysyl oxidase-like gene (LOXL). Oligonucleotides complementary to conserved domains within exons 4 and 5 of the human lysyl oxidase-like gene were used to amplify the corresponding segment from mouse genomic DNA. Sequencing of the resulting mouse DNA fragment of approximately 1 kb revealed that the exon sequences at the ends of the amplified fragment are highly homologous (90% nucleotide identity) to exons 4 and 5 of the human lysyl oxidase-like gene. An AluI restriction site polymorphism within intron 4 was used to map the mouse lysyl oxidase-like gene (Loxl) to mouse Chromosome 9 in a region that shares linkage conservation with human chromosome 15q24, to which the LOXL was recently mapped.
一种涉及使用聚合酶链反应的内含子捕获策略被用于鉴定和定位人赖氨酰氧化酶样基因(LOXL)的小鼠同源基因。与人赖氨酰氧化酶样基因外显子4和5内保守结构域互补的寡核苷酸被用于从小鼠基因组DNA中扩增相应片段。对所得约1 kb的小鼠DNA片段进行测序,结果显示扩增片段末端的外显子序列与人赖氨酰氧化酶样基因的外显子4和5高度同源(核苷酸同一性为90%)。内含子4内的一个AluI限制性位点多态性被用于将小鼠赖氨酰氧化酶样基因(Loxl)定位到小鼠9号染色体上的一个区域,该区域与人类15号染色体q24共享连锁保守性,而LOXL最近被定位到该染色体上。