Isobe M, Koyata H, Sakakibara T, Momoi-Isobe K, Hiraga K
Department of Patho-Biochemistry, Research Institute for Oriental Medicine, Toyama, Japan.
Biochem Biophys Res Commun. 1994 Sep 30;203(3):1483-7. doi: 10.1006/bbrc.1994.2352.
Southern analysis using a human glycine decarboxylase cDNA probe and genomic DNA preparations from Chinese hamster-human hybridoma cell lines demonstrated that on the segregated human chromosomes, 4 and 9, there are glycine decarboxylase cDNA-related sequences. The finding is confirmatory of the fact that fragments of both the true and processed genes for this protein have been cloned. Since one of four HindIII fragments revealed in the present Southern analysis matched requirements for the property expected from the restriction map reported for the processed gene, this was located on chromosome 4. The three remaining signals were consequently ascribed to fragments from the true gene on chromosome 9. Fluorescence in situ hybridization using the genomic clones assigned the true and processed genes to 9p23-24 and 4q12, respectively.
使用人甘氨酸脱羧酶cDNA探针和来自中国仓鼠-人杂交瘤细胞系的基因组DNA制剂进行的Southern分析表明,在分离的人类染色体4和9上,存在与甘氨酸脱羧酶cDNA相关的序列。这一发现证实了该蛋白质的真实基因和加工基因的片段均已被克隆这一事实。由于在本次Southern分析中揭示的四个HindIII片段之一符合已报道的加工基因限制性图谱所预期的特性要求,因此该片段位于4号染色体上。其余三个信号因此归因于9号染色体上真实基因的片段。使用基因组克隆进行的荧光原位杂交分别将真实基因和加工基因定位到9p23 - 24和4q12。