Minfeng Fang

Minfeng Fang


Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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Verified
Journal Article
Open access
PDF file
WDWan-Lin Dong
Wan-Lin Dong
RWRuo-Nan Wang
Ruo-Nan Wang
NZNa-Yao Zhang
Na-Yao Zhang
WFWei-Bing Fan
Wei-Bing Fan
MFMinfeng Fang
Minfeng Fang
ZLZhonghu Li
Zhonghu Li
Orchidaceae is the 3rd largest family of angiosperms, an evolved young branch of monocotyledons. This family contains a number of economically-important horticulture and flowering plants. However, the limited availability of genomic information largely hindered the study of molecular evolution and phylogeny of Orchidaceae. In this study, we determined the evolutionary characteristics of whole chloroplast (cp) genomes and the phylogenetic relationships of the family Orchidaceae. We firstly characterized the cp genomes of four orchid species: Cremastra appendiculata, Calanthe davidii, Epipactis mairei, and Platanthera japonica. The size of the chloroplast genome ranged from 153,629 bp (C. davidi) to 160,427 bp (E. mairei). The gene order, GC content, and gene compositions are similar to those of other previously-reported angiosperms. We identified that the genes of ndhC, ndhI, and ndhK were lost in C. appendiculata, in that the ndh I gene was lost in P. japonica and E. mairei. In addition, the four types of repeats (forward, palindromic, reverse, and complement repeats) were examined in orchid species. E. mairei had the highest number of repeats (81), while C. davidii had the lowest number (57). The total number of Simple Sequence Repeats is at least 50 in C. davidii, and, at most, 78 in P. japonica. Interestingly, we identified 16 genes with positive selection sites (the psbH, petD, petL, rpl22, rpl32, rpoC1, rpoC2, rps12, rps15, rps16, accD, ccsA, rbcL, ycf1, ycf2, and ycf4 genes), which might play an important role in the orchid species’ adaptation to diverse environments. Additionally, 11 mutational hotspot regions were determined, including five non-coding regions (ndhB intron, ccsA-ndhD, rpl33-rps18, ndhE-ndhG, and ndhF-rpl32) and six coding regions (rps16, ndhC, rpl32, ndhI, ndhK, and ndhF). The phylogenetic analysis based on whole cp genomes showed that C. appendiculata was closely related to C. striata var. vreelandii, while C. davidii and C. triplicate formed a small monophyletic evolutionary clade with a high bootstrap support. In addition, five subfamilies of Orchidaceae, Apostasioideae, Cypripedioideae, Epidendroideae, Orchidoideae, and Vanilloideae, formed a nested evolutionary relationship in the phylogenetic tree. These results provide important insights into the adaptive evolution and phylogeny of Orchidaceae.

1 February 2019 in Plant Diversity
Verified
Journal Article
Open access
YJYun Jia
Yun Jia
JBJi-Qing Bai
Ji-Qing Bai
MLMi-Li Liu
Mi-Li Liu
ZJZhen-Fang Jiang
Zhen-Fang Jiang
YWYan Wu
Yan Wu
ZLZhonghu Li
Zhonghu Li
Notopterygium incisum C. C. Ting ex H. T. Chang (Apiaceae) is an endangered perennial herb in China. The lack of transcriptomic and genomic resources for N. incisum greatly hinders studies of its population genetics and conservation. In this study, we employed RNA-seq technology to characterize transcriptomes for the flowers, leaves, and stems of this endangered herb. A total of 56 million clean reads were assembled into 120,716 unigenes with an N50 length of 850 bp. Among these unigenes, 70,245 (58.19%) were successfully annotated and 65,965 (54.64%) were identified as coding sequences based on their similarities with sequences in public databases. We identified 21 unigenes that had significant relationships with cold tolerance in N. incisum according to gene ontology (GO) annotation analysis. In addition, 13,149 simple sequence repeats (SSRs) and 85,681 single nucleotide polymorphisms were detected as potential molecular genetic markers. Ninety-six primer pairs of SSRs were randomly selected to validate their amplification efficiency and polymorphism. Nineteen SSR loci exhibited polymorphism in three natural populations of N. incisum. These results provide valuable resources to facilitate future functional genomics and conservation genetics studies of N. incisum.

1 April 2017 in Biochemical Systematics and Ecology
Verified
Journal Article
Closed access
YHYan-Ling He
Yan-Ling He
YHYing He
Ying He
LGLin-Lin Gong
Lin-Lin Gong
MFMinfeng Fang
Minfeng Fang
ZLZhonghu Li
Zhonghu Li

27 October 2017 in Conservation Genetics Resources
Verified
Journal Article
Closed access
PDF file
YWYing Wu
Ying Wu
TZTian-Ze Zhang
Tian-Ze Zhang
DQDai-Yu Qiu
Dai-Yu Qiu
QCQiang Chai
Qiang Chai
WFWei-Bing Fan
Wei-Bing Fan
MFMinfeng Fang
Minfeng Fang

3 July 2019 in Mitochondrial DNA Part B
Verified
Journal Article
Open access
PDPeng-Bin Dong
Peng-Bin Dong
YLYu Liu
Yu Liu
QGQi-Yuan Gao
Qi-Yuan Gao
TYTing Yang
Ting Yang
XCXue-Yi Chen
Xue-Yi Chen
MFMinfeng Fang
Minfeng Fang
Acer tsinglingense is an ecologically and economically important tree species in China. In this study, we characterized its whole plastid genome sequence using the Illumina sequencing platform. The complete plastid genome size of A. tsinglingense is 156,039 bp in length, including a large single-copy [LSC] region of 85,760 bp, a small single-copy [SSC] region of 18,139 bp, and a pair of inverted repeats [IRs] of 26,070 bp. The genome contains 137 genes, including 89 protein-coding genes, 40 tRNA genes, and 8 rRNA genes. The GC contents in chloroplast genome, LSC region, SSC region, and IR region were 38.0%, 36.2%, 32.4%, and 42.9%, respectively. The phylogenetic analysis based on the plastid genomes showed that A. tsinglingense was more closely related with the congeneric A. laevigatum, A. palmatum, A. wilsonii, and A. buergerianum, these species were clustered into a monophyletic clade with high bootstrap support.

17 February 2024 in Journal of Pharmaceutical and Biomedical Analysis
Verified
Journal Article
Closed access
XLXuechao Li
Xuechao Li
WYWen Yang
Wen Yang
YLYu Li
Yu Li
JKJing Kang
Jing Kang
JWJing Wang
Jing Wang
MFMinfeng Fang
Minfeng Fang