Establishment of a Bone-Specific col10a1:GFP Transgenic Zebrafish

斑马鱼 绿色荧光蛋白 转基因 细胞生物学 生物 遗传学 基因
作者
Yong‐Il Kim,Suman Lee,Seung-Hyun Jung,Hyun-Taek Kim,Jung‐Hwa Choi,Mi‐Sun Lee,Kwan‐Hee You,Sang‐Yeob Yeo,Kyeong‐Won Yoo,SeongAe Kwak,Joon No Lee,Raekil Park,Seong‐Kyu Choe,Cheol‐Hee Kim
出处
期刊:Molecules and Cells [Springer Science+Business Media]
卷期号:36 (2): 145-150 被引量:52
标识
DOI:10.1007/s10059-013-0117-7
摘要

Elucidation of the roles of circadian associated factors requires a better understanding of the molecular mechanisms of circadian rhythms, control of flowering time through photoperiodic pathways, and photosensory signal transduction. In Arabidopsis, the APRR1 quintet, APRRs 1, 3, 5, 7, and 9, are known as central oscillator genes. Other plants may share the molecular mechanism underlying the circadian rhythm. To identify and characterize these circadian response genes in Brassica crops whose genome was triplicated after divergence from Arabidopsis, we identified B. rapa BAC clones containing these genes by BLAST analysis of B. rapa BAC end sequences against the five corresponding Arabidopsis regions. Subsequent fingerprinting, Southern hybridization, and PCR allowed identification of five BAC clones, one for each of the five circadian-related genes. By draft shotgun sequencing of the BAC clones, we identified the complete gene sequences and cloned the five expressed B. rapa circadian-associated gene members, BrPRRs 1, 3, 5, 7, and 9. Phylogenetic analysis revealed that each BrPRR was orthologous to the corresponding APRR at the sequence level. Northern hybridization revealed that the five genes were transcribed at distinct points in the 24 hour period, and Southern hybridization revealed that they are present in 2, 1, 2, 2, and 1 copies, respectively in the B. rapa genome, which was triplicated and then diploidized during the last 15 million years.

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