Genome-wide In Silico Analysis, Characterization and Identification of Microsatellites in Spodoptera littoralis Multiple nucleopolyhedrovirus (SpliMNPV)

被引:16
|
作者
Atia, Mohamed A. M. [1 ]
Osman, Gamal H. [2 ,3 ]
Elmenofy, Wael H. [3 ]
机构
[1] ARC, AGERI, Genome Mapping Dept, Giza 12619, Egypt
[2] Umm Al Qura Univ, Biol Dept, Fac Sci Appl, POB 715, Mecca 21955, Saudi Arabia
[3] ARC, AGERI, Microbial Genet Dept, Giza, Egypt
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
SIMPLE SEQUENCE REPEATS; DIFFERENTIAL DISTRIBUTION; MONONUCLEOTIDE REPEATS; ESCHERICHIA-COLI; DNA; GENE; POLYMORPHISM; DELETIONS; MUTATION; VIRUSES;
D O I
10.1038/srep33741
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In this study, we undertook a survey to analyze the distribution and frequency of microsatellites or Simple Sequence Repeats (SSRs) in Spodoptera littoralis multiple nucleopolyhedrovirus (SpliMNPV) genome (isolate AN-1956). Out of the 55 microsatellite motifs, identified in the SpliMNPV-AN1956 genome using in silico analysis (inclusive of mono-, di-, tri- and hexa-nucleotide repeats), 39 were found to be distributed within coding regions (cSSRs), whereas 16 were observed to lie within intergenic or noncoding regions. Among the 39 motifs located in coding regions, 21 were located in annotated functional genes whilst 18 were identified in unknown functional genes (hypothetical proteins). Among the identified motifs, trinucleotide (80%) repeats were found to be the most abundant followed by dinucleotide (13%), mononucleotide (5%) and hexanucleotide (2%) repeats. The 39 motifs located within coding regions were further validated in vitro by using PCR analysis, while the 21 motifs located within known functional genes (15 genes) were characterized using nucleotide sequencing. A comparison of the sequence analysis data of the 21 sequenced cSSRs with the published sequences is presented. Finally, the developed SSR markers of the 39 motifs were further mapped/ localized onto the SpliMNPV-AN1956 genome. In conclusion, the SSR markers specific to SpliMNPV, developed in this study, could be a useful tool for the identification of isolates and analysis of genetic diversity and viral evolutionary status.
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页数:9
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