详细信息
Complete Chloroplast Genome Sequence of Decaisnea insignis: Genome Organization, Genomic Resources and Comparative Analysis ( SCI-EXPANDED收录) 被引量:44
文献类型:期刊文献
英文题名:Complete Chloroplast Genome Sequence of Decaisnea insignis: Genome Organization, Genomic Resources and Comparative Analysis
作者:Li, Bin[1,2,3] Lin, Furong[1,2,3] Huang, Ping[1,2,3] Guo, Wenying[1,2,3] Zheng, Yongqi[1,2,3]
第一作者:李斌
通信作者:Zheng, YQ[1];Zheng, YQ[2];Zheng, YQ[3]
机构:[1]Chinese Acad Forestry, State Key Lab Tree Genet & Breeding, Beijing, Peoples R China;[2]Chinese Acad Forestry, Res Inst Forestry, Beijing, Peoples R China;[3]Chinese Acad Forestry, State Forestry Adm, Key Lab Tree Breeding & Cultivat, Beijing, Peoples R China
年份:2017
卷号:7
期号:1
外文期刊名:SCIENTIFIC REPORTS
收录:;WOS:【SCI-EXPANDED(收录号:WOS:000408622400167)】;
基金:This work was supported by the National Forest Gerplasm Resources Shared Service Platform 2016.
语种:英文
摘要:Decaisnea insignis is a wild resource plant and is used as an ornamental, medicinal, and fruit plant. High-throughput sequencing of chloroplast genomes has provided insight into the overall evolutionary dynamics of chloroplast genomes and has enhanced our understanding of the evolutionary relationships within plant families. In the present study, we sequenced the complete chloroplast genome of D. insignis and used the data to assess its genomic resources. The D. insignis chloroplast genome is 158,683 bp in length and includes a pair of inverted repeats of 26,167 bp that are separated by small and large single copy regions of 19,162 bp and 87,187 bp, respectively. We identified 83 simple sequence repeats and 18 pairs of large repeats. Most simple-sequence repeats were located in the noncoding sections of the large single-copy/small single-copy region and exhibited a high A/T content. The D. insignis chloroplast genome bias was skewed towards A/T on the basis of codon usage. A phylogenetic tree based on 82 protein-coding genes of 33 angiosperms showed that D. insignis was clustered with Akebia in Lardizabalaceae. Overall, the results of this study will contribute to better understanding the evolution, molecular biology and genetic improvement of D. insignis.
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