Construction and characterization of the infectious clone of porcine parvovirus carrying genetic marker

2019 ◽  
Vol 235 ◽  
pp. 143-150 ◽  
Author(s):  
Songbiao Chen ◽  
Bichen Miao ◽  
Huan Zhang ◽  
Yingli Xiong ◽  
Xiujuan Zhang ◽  
...  
2012 ◽  
Vol 167 (2) ◽  
pp. 146-151 ◽  
Author(s):  
Xiaoyun Deng ◽  
Xiaole Qi ◽  
Guan Wu ◽  
Yulong Gao ◽  
Liting Qin ◽  
...  

PLoS ONE ◽  
2012 ◽  
Vol 7 (11) ◽  
pp. e50413 ◽  
Author(s):  
Felipe L. Assis ◽  
Gabriel M. F. Almeida ◽  
Danilo B. Oliveira ◽  
Ana P. M. Franco-Luiz ◽  
Rafael K. Campos ◽  
...  

2007 ◽  
Vol 2007 ◽  
pp. 156-156 ◽  
Author(s):  
Masoud Alipanah ◽  
Lobov Kalashnikova ◽  
Genadi Rodionov

Prolactin plays an important regulatory function in mammary gland development, milk secretion, and expression of milk protein genes. Hence the PRL gene is a potential genetic marker of production traits in dairy cattle. The gene was mapped on chromosome 23 by Hallerman et al. (1988). It consists of 5 exons and four introns (Camper et al. 1984) encoding the 199-amino-acid mature protein (Wallis 1974). On the basis of sequence analysis of four different cDNA clones, seven possible nucleotide substitutions were described by Sasavage et al. (1982). One of them, recognized by RsaI endonuclease, has become a popular genetic marker used for genetic characterization of cattle populations by means of PCR-RFLP (Mitra et al., 1995). Two allelic variants (B and b) have been distinguished at the DNA level, based on RsaI polymorphism in the third exon of the coding region. It has been suggested that prolactin alleles correlate with milk yield (Lewin et al., 1992).


2020 ◽  
Vol 17 (1) ◽  
Author(s):  
Hui-Hua Zheng ◽  
Lin-Qing Wang ◽  
Peng-Fei Fu ◽  
Lan-Lan Zheng ◽  
Hong-Ying Chen ◽  
...  

2013 ◽  
Vol 94 (2) ◽  
pp. 219-224 ◽  
Author(s):  
Yi G. Xu ◽  
Li C. Cui ◽  
Hong W. Wang ◽  
Gui C. Huo ◽  
Su L. Li

2020 ◽  
Vol 2 (1) ◽  
Author(s):  
Mingmin Zhao ◽  
Beatriz García ◽  
Araiz Gallo ◽  
Ioannis E. Tzanetakis ◽  
Carmen Simón-Mateo ◽  
...  

AbstractAn unprecedented number of viruses have been discovered by leveraging advances in high-throughput sequencing. Infectious clone technology is a universal approach that facilitates the study of biology and role in disease of viruses. In recent years homology-based cloning methods such as Gibson assembly have been used to generate virus infectious clones. We detail herein the preparation of home-made cloning materials for Gibson assembly. The home-made materials were used in one-step generation of the infectious cDNA clone of a plant RNA virus into a T-DNA binary vector. The clone was verified by a single Illumina reaction and a de novo read assembly approach that required no primer walking, custom primers or reference sequences. Clone infectivity was finally confirmed by Agrobacterium-mediated delivery to host plants. We anticipate that the convenient home-made materials, one-step cloning and Illumina verification strategies described herein will accelerate characterization of viruses and their role in disease development.


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