Stage-specific reference genes significant for quantitative PCR during mouse retinal development

被引:18
作者
Adachi, Hiroko [1 ]
Tominaga, Hiroyuki [1 ]
Maruyama, Yuko [2 ]
Yoneda, Kazuhito [2 ]
Maruyama, Kazuichi [2 ]
Yoshii, Kengo [3 ]
Kinoshita, Shigeru [2 ]
Nakano, Masakazu [1 ]
Tashiro, Kei [1 ]
机构
[1] Kyoto Prefectural Univ Med, Dept Genom Med Sci, Kyoto 6028566, Japan
[2] Kyoto Prefectural Univ Med, Dept Ophthalmol, Kyoto 6028566, Japan
[3] Kyoto Prefectural Univ Med, Dept Med Stat, Kyoto 6028566, Japan
关键词
REAL-TIME PCR; HOUSEKEEPING GENES; EXPRESSION; VEGF; DISEASE; MODEL; NEOVASCULARIZATION; SELECTION; CELLS;
D O I
10.1111/gtc.12254
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Developing mouse retina has been serving as an ideal model for investigating the molecular mechanism of neural development and angiogenesis, because several significant events associated with these physiological phenomena are drastically occurring in conjunction with retinal development. However, as many genes are influencing on each other to establish mature retina within 21days from E10 to P12, we must carefully design the experiments, such as in the case of quantitating the amount of altered gene expression toward the establishment of retina by quantitative PCR. As we have seen considerable variations of quantitative results in different developmental stages of retina depending on the reference genes used for compensation, we here attempted to determine a reliable reference gene to accurately quantitate the target genes in each stage. According to the results of in silico prediction and comparison with a database of SAGE, we found that the most stable gene from early to late stages was Sdha, whereas one of the most popular housekeeping genes, Actb, was the one that could mislead the quantitative results even in the adult stage. Consequently, we pointed out the importance of selecting an appropriate reference gene, especially to quantitate the amount of gene expression in the developmental stages of a certain tissue.
引用
收藏
页码:625 / 635
页数:11
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