scholarly journals Efficient amplification of self-gelling polypod-like structured DNA by rolling circle amplification and enzymatic digestion

2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Tomoya Yata ◽  
Yuki Takahashi ◽  
Mengmeng Tan ◽  
Kumi Hidaka ◽  
Hiroshi Sugiyama ◽  
...  

Abstract The application of DNA as a functional material such as DNA hydrogel has attracted much attention. Despite an increasing interest, the high cost of DNA synthesis is a limiting factor for its utilization. To reduce the cost, we report here a highly efficient amplification technique for polypod-like structured DNA (polypodna) with adhesive ends that spontaneously forms DNA hydrogel. Two types of polypodna with three (tripodna) and four (tetrapodna) pods were selected and a template oligodeoxynucleotide, containing a tandem sequence of a looped tripodna or tetrapodna, respectively, along with restriction enzyme (TspRI) sites, was designed. The template was circularized using T4 DNA ligase and amplified by rolling circle amplification (RCA). The RCA product was highly viscous and resistant to restriction digestion. Observation under an electron microscope revealed microflower-like structures. These structures were composed of long DNA and magnesium pyrophosphate and their treatment with EDTA followed by restriction digestion with TspRI resulted in numerous copies of polypodna with adhesive ends, which formed a DNA hydrogel. Thus, we believe this technique provides a new approach to produce DNA nanostructures and helps in expanding their practical applications.

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Tomoya Yata ◽  
Yuki Takahashi ◽  
Mengmeng Tan ◽  
Kumi Hidaka ◽  
Hiroshi Sugiyama ◽  
...  

2019 ◽  
Vol 11 (15) ◽  
pp. 2082-2088 ◽  
Author(s):  
Zhanmin Liu ◽  
Yanming Wang ◽  
Liping Li ◽  
Junhai Li ◽  
Yuanyuan Yuan

MicroRNA-378 (miRNA-378) is widely regarded as a novel noninvasive serum biomarker for early detection of gastric cancer.


2019 ◽  
Vol 11 (36) ◽  
pp. 4629-4636
Author(s):  
Hongxin Jiang ◽  
Guimei Han ◽  
Yaping Xu ◽  
Junxing Li ◽  
Xiaowei Liu ◽  
...  

A fluorescent sensing strategy for ultrasensitive and highly selective detection of ATP was presented by taking advantage of the exponential amplification capability of BRCA and the extreme specificity of T4 DNA ligase toward ATP.


2003 ◽  
pp. 51-63 ◽  
Author(s):  
Paul M. Richardson ◽  
Chris Detter ◽  
Barry Schweitzer ◽  
Paul F. Predki

2017 ◽  
Vol 23 (72) ◽  
pp. 18276-18281 ◽  
Author(s):  
Wanlin Xu ◽  
Yishun Huang ◽  
Haoran Zhao ◽  
Pan Li ◽  
Guoyuan Liu ◽  
...  

Talanta ◽  
2019 ◽  
Vol 192 ◽  
pp. 175-181 ◽  
Author(s):  
Huo Xu ◽  
Shuxin Zhang ◽  
Changhe Ouyang ◽  
Zhenmeng Wang ◽  
Dong Wu ◽  
...  

Plant Disease ◽  
2012 ◽  
Vol 96 (1) ◽  
pp. 149-149 ◽  
Author(s):  
M. S. Ali-Shtayeh ◽  
R. M. Jamous ◽  
E. Y. Hussein ◽  
O. B. Mallah ◽  
S. Y. Abu-Zaitoun

In the summer of 2010, watermelon plants (Citrullus lanatus Thunb.) from eight fields surveyed in two districts (Jenin and Qalqilia) in the West Bank of the Palestinian Authority (PA) exhibited typical Watermelon chlorotic stunt virus (WmCSV) symptoms including yellow veining, chlorotic mottling, stunting of young leaves, and reduction of yield. Disease incidence ranged from 8 to 98% and was associated with whitefly (Bemisia tabaci) infestation. In symptomatic leaves of 79 of 215 watermelon plants examined, geminiviral DNA was detected by PCR (3) and rolling circle amplification (RCA) (2). Geminivirus DNA-A and DNA-B component fragments were amplified by PCR using degenerated and specific primers (3). The full-length DNA-A of WmCSV-[PAL] was amplified from field-collected watermelon plants using WAI-XbaI-(v)/WAI-XbaI-(c) primer pair, and the generated PCR product was sequenced (3). A DNA-A fragment (2,017 bp) (GenBank Accession No JN673223) comprising a conserved region of the coat protein (AV1), AC5, AC3, AC1, and AC2 genes, showed 99, 99, 99, 98, 98, and 97% nucleotide identity with sequences of WmCSV isolates from Jordan (GenBank Accession No. EU561237), Israel (LEF201809), Lebanon (HM368371), Sudan (AJ245650), Iran (AJ245652), and Yemen (AJ012081), respectively. The circular genomic DNA-A and DNA-B of WmCSV-[PAL] were amplified from a whitefly-inoculated watermelon plant by RCA (2) and used to inoculate 30 watermelon plants with a nonvacuum gene gun (4). Typical WmCSV symptoms developed in all these plants 4 weeks postinoculation and virus infection was confirmed by PCR. In 2011, WmCSV was detected from the southern and eastern parts of neighboring Jordan (1). The new emergent disease in the PA was detected in all of the surveyed watermelon fields in regions where cucurbits are intensively grown, only a few kilometers east of Israel. This suggests that the introduction of WmCSV to the PA might have occurred through transplant movement between Israel and the PA or through viruliferous whiteflies that moved from infected plants in Israel to neighboring fields in Jenin and Qalqilia districts. This is in accordance with the observation that disease incidence was always associated with high population of B. tabaci. The virus endangers the production of watermelon in the affected areas to the point of becoming the limiting factor of growing watermelon in open fields. To our knowledge, this is the first report of WmCSV infecting cucurbits in the PA. References: (1) A. Al-Musa et al. Virus Genes 43:79, 2011. (2) H. Jeske. Curr. Topics Microbiol. Immunol. 331:185, 2009. (3) A. Kheyr-Pour et al. Phytopathology 90:629, 2000. (4) S. Sikorskaite et al. J. Virol. Methods 165:320, 2010.


2014 ◽  
Vol 50 (86) ◽  
pp. 13049-13051 ◽  
Author(s):  
Cheol Am Hong ◽  
Bora Jang ◽  
Eun Hye Jeong ◽  
Hansaem Jeong ◽  
Hyukjin Lee

Large-scale preparation of DNA nanostructures for siRNA delivery has been achieved by an isothermal enzymatic amplification process.


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