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2014 Vol. 41, No. 1

Research article
Editorial
Yongbiao Xue
2014, 41(1): 1-2. doi: 10.1016/j.jgg.2014.01.002
Abstract (62) HTML PDF (3)
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News and views
Evolution of Influenza A H7N9 Virus with an Emphasis on Gene Constellation
Zifeng Yang, Runfeng Li, Tianyu Zhang
2014, 41(1): 3-6. doi: 10.1016/j.jgg.2013.12.005
Abstract (70) HTML PDF (0)
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Review
CRISPR/Cas9 and Genome Editing in Drosophila
Andrew R. Bassett, Ji-Long Liu
2014, 41(1): 7-19. doi: 10.1016/j.jgg.2013.12.004
Abstract (61) HTML PDF (1)
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Recent advances in our ability to design DNA binding factors with specificity for desired sequences have resulted in a revolution in genetic engineering, enabling directed changes to the genome to be made relatively easily. Traditional techniques for generating genetic mutations in most organisms have relied on selection from large pools of randomly induced mutations for those of particular interest, or time-consuming gene targeting by homologous recombination. Drosophila melanogaster has always been at the forefront of genetic analysis, and application of these new genome editing techniques to this organism will revolutionise our approach to performing analysis of gene function in the future. We discuss the recent techniques that apply the CRISPR/Cas9 system to Drosophila, highlight potential uses for this technology and speculate upon the future of genome engineering in this model organism.
Methylation Modifications in Eukaryotic Messenger RNA
Jun Liu, Guifang Jia
2014, 41(1): 21-33. doi: 10.1016/j.jgg.2013.10.002
Abstract (74) HTML PDF (1)
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RNA methylation modifications have been found for decades of years, which occur at different RNA types of numerous species, and their distribution is species-specific. However, people rarely know their biological functions. There are several identified methylation modifications in eukaryotic messenger RNA (mRNA), such as N7-methylguanosine (m7G) at the cap, N6-methyl-2′-O-methyladenosine (m6Am), 2′-O-methylation (Nm) within the cap and the internal positions, and internal N6-methyladenosine (m6A) and 5-methylcytosine (m5C). Among them, m7G cap was studied more clearly and found to have vital roles in several important mRNA processes like mRNA translation, stability and nuclear export. m6A as the most abundant modification in mRNA was found in the 1970s and has been proposed to function in mRNA splicing, translation, stability, transport and so on. m6A has been discovered as the first RNA reversible modification which is demethylated directly by human fat mass and obesity associated protein (FTO) and its homolog protein, alkylation repair homolog 5 (ALKBH5). FTO has a special demethylation mechanism that demethylases m6A to A through two over-oxidative intermediate states: N6-hydroxymethyladenosine (hm6A) and N6-formyladenosine (f6A). The two newly discovered m6A demethylases, FTO and ALKBH5, significantly control energy homeostasis and spermatogenesis, respectively, indicating that the dynamic and reversible m6A, analogous to DNA and histone modifications, plays broad roles in biological kingdoms and brings us an emerging field “RNA Epigenetics”. 5-methylcytosine (5mC) as an epigenetic mark in DNA has been studied widely, but m5C in mRNA is seldom explored. The bisulfide sequencing showed m5C is another abundant modification in mRNA, suggesting that it might be another RNA epigenetic mark. This review focuses on the main methylation modifications in mRNA to describe their formation, distribution, function and demethylation from the current knowledge and to provide future perspectives on functional studies.
Original research
miR-888 in MCF-7 Side Population Sphere Cells Directly Targets E-cadherin
Shengjian Huang, Ming Cai, Yinghui Zheng, Longhai Zhou, Qiang Wang, Liangbiao Chen
2014, 41(1): 35-42. doi: 10.1016/j.jgg.2013.12.002
Abstract (61) HTML PDF (9)
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Side population (SP) cells are a small subset of cells isolated from a cultured cancer cell line that exhibit characteristics similar to those of cancer stem cells (CSCs), such as high metastatic and tumorigenic potential. The molecular mechanisms that give rise to the malignant properties of SP cells are not clear. We isolated SP cells from the MCF-7 breast cancer cell line and profiled microRNA (miRNA) expression patterns between SP cell-derived spheroids and non-SP cells. SP spheroids were found to possess 42 up-regulated miRNAs and 27 down-regulated ones (above 5-fold changes). One of the up-regulated miRNAs, miR-888 computationally predicted to participate in the adherens junction (AJ) pathway, was investigated. Over-expression of miR-888 in MCF-7 cells reduced the mRNA levels of all four AJ pathway genes (E-cadherin, ACTG1, PTPRT and CDC42) that were selected for testing, whereas knocking down miR-888 reversed the trends. Western blot and flow cytometric quantitation of the membrane E-cadherin levels showed the same trend of change under these treatments. Luciferase reporter assay showed E-cadherin is a direct target of miR-888. As a potential role in intercellular adhesiveness and maintenance of malignant tissue architecture, the results indicate that miR-888 is a repressor of the AJ pathway in MCF-7 cells and that up-regulation of miR-888 contributes to aggressiveness in MCF-7 SP cells.
Letter to the Editor
Efficient Gene Targeting in Zebrafish Mediated by a Zebrafish-Codon-Optimized Cas9 and Evaluation of Off-Targeting Effect
Da Liu, Zhanxiang Wang, An Xiao, Yutian Zhang, Wenyuan Li, Yao Zu, Shaohua Yao, Shuo Lin, Bo Zhang
2014, 41(1): 43-46. doi: 10.1016/j.jgg.2013.11.004
Abstract (67) HTML PDF (3)
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