Abstract
The complete chloroplast genome of Leptochilus hemionitideus was sequenced. Its length is 156,083 bp with 44.2% GC content. The genome exhibits typical quadripartite with two inverted repeat regions (24,594 bp, each) separated by a large single-copy (LSC, 81,403 bp) region and a small single-copy (SSC, 25,492 bp) region. It has 131 genes, including 87 protein-coding genes, 34 tRNA genes, eight rRNA genes and two pseudogenes. Maximum-likelihood phylogenetic tree indicated that L. hemionitideus was closely related to Lepisorus clathratus. The complete chloroplast genome of L. hemionitideus would provide very valuable molecular information for further inferring the relationships of the microsoroid ferns.
Keywords: Leptochilus hemionitideus, chloroplast genome, phylogenetic analysis
Leptochilus hemionitideus is terrestrial fern belonging to the subfamily Microsoroideae in Polypodiaceae (Zhang et al. 2013). Different from congeneric other species, it has orbicular to elongate sori on tertiary veins parallel to secondary veins (Zhang et al. 2013). Its fronds are not or only slightly dimorphic. The plant has rock habit, usually growing on stones in streams at an altitude of 700–2000 m (Zhang et al. 2013). Its main distribution areas are concentrated in China, Bhutan, India, Japan, Nepal and Thailand (Zhang et al. 2013). In China, L. hemionitideus is a traditional Chinese medical fern with clearing heat and detoxification (State Administration of Traditional Chinese Medicine ‘Chinese Materia Medica Committee’ 1999). In addition, whether Leptochilus were merged with Colysis occurs controversy due to lack of the obvious generic delimitation (Nooteboom 1997; Shi and Zhang 1999). Phylogenetic relationships of Leptochilus to some genera in Microsoroideae such as Microsorum are also needed to further explore (Christenhusz and Chase 2014; PPG I 2016). Therefore, sequencing complete chloroplast genome of L. hemionitideus will contribute to deal with these issues and lay solid foundations for further phylogenomic investigation.
We sampled fresh and young leaves of L. hemionitideus from South China Botanical Garden, Chinese Academy of Sciences (CAS; 23°11′3.56″N, 113°21′43.28″E). The voucher specimen was conserved in Herbarium of Sun Yat-sen University (SYS; voucher: SS Liu 20161014). After total genomic DNA extraction, we built up ∼300 bp genomic library and sequenced in Illumina Hiseq 2500 platform (Illumina Inc., San Diego, CA). Total 8,119,002 raw reads were retrieved and trimmed by Trimmomatic (Bolger et al. 2014). A subset of 6,801,257 trimmed reads was used for reconstructing the chloroplast genome by Velvet v1.2.07 (Zerbino and Birney 2008) with 33× coverage. The chloroplast genome was annotated using DOGMA (Wyman et al. 2004) and tRNAscan-SE (Schattner et al. 2005) programs with default settings and finally validated with BLAST searches and manually corrected for intron/exon boundaries. The complete chloroplast genome sequence of L. hemionitideus was aligned with 11 representative ferns including Marsilea crenata as outgroup using MAFFT v7.311 (Katoh and Standley 2013). A maximum likelihood (ML) phylogenetic tree was constructed using RAxML v.8.0 with 1000 bootstrap replicates (Stamatakis 2014).
We determined complete chloroplast genome of L. hemionitideus, which possesses a total length of 156,083 bp with 44.2% GC content (GenBank accession number: MH319943). The circular cp genome exhibits typical quadripartite with two inverted repeat regions (IRa and IRb) of 24,594 bp separated by a large single-copy (LSC) region of 81,403 bp and a small single-copy (SSC) region of 25,492 bp. It was predicted to contain 131 genes, including 87 protein-coding genes, 34 tRNA genes, eight rRNA genes and two pseudogenes (ndhB and rpoC1). Among them, 115 genes occur as a single copy, whereas 14 genes are duplicated in the IR regions. Fourteen genes contain one intron, especially, the gene ycf3, clpP, and rps12 have two introns. ML tree indicated that L. hemionitideus is closely related to Lepisorus clathratus (Figure 1). The complete chloroplast genome of L. hemionitideus will provide very valuable molecular information for further inferring the relationships of the microsoroid ferns.
Figure 1.
ML phylogenetic tree inferred based on complete chloroplast genomes of 12 representative ferns including Marsilea crenata as outgroup. Node labels indicate the bootstrap support values with 1000 replicates.
Disclosure statement
No potential conflict of interest was reported by the authors.
References
- Bolger AM, Lohse M, Usadel B. 2014. Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics. 30:2114–2120. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Christenhusz MJ, Chase MW. 2014. Trends and concepts in fern classification. Ann Bot. 113:571–594. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Katoh K, Standley DM. 2013. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol Biol Evol. 30:772–780. [DOI] [PMC free article] [PubMed] [Google Scholar]
- PPG I 2016. A community-derived classification for extant lycophytes and ferns. J Sytem Evol. 54:563–603. [Google Scholar]
- Shi L, Zhang XC. 1999. Taxonomic studies of the genus Colysis C. Presl (Polypodiaceae) from China and neighboring regions. Acta Phytotaxon Sin. 37:54–80. [Google Scholar]
- State Administration of Traditional Chinese Medicine ‘Chinese Materia Medica Committee’ 1999. Zhong Hua Ben Cao [Chinese Materia Medica], Vol. 4 Shanghai: Shanghai Science and Technology Publisher; p. 223–224. [Chinese] [Google Scholar]
- Schattner P, Brooks AN, Lowe TM. 2005. The tRNAscan-SE, snoscan and snoGPS web servers for the detection of tRNAs and snoRNAs. Nucleic Acids Res. 33:W686–W689. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nooteboom H. 1997. The microsoroid ferns. Blumea. 42:261–395. [Google Scholar]
- Stamatakis A. 2014. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics. 30:1312–1313. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wyman SK, Jansen RK, Boore JL. 2004. Automatic annotation of organellar genomes with DOGMA. Bioinformatics. 20:3252–3255. [DOI] [PubMed] [Google Scholar]
- Zerbino DR, Birney E. 2008. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res. 18:821–829. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhang XC, Lu SG, Lin YX, Qi XP, Moore S, Xing FW, Wang FG, Hovenkamp PH, Gilbert MG, Nooteboom HP, et al. 2013. Polypodiaceae In: Wu ZY, Raven PH, Hong DY, eds., Flora of China. Vol. 2–3(Pteridophytes) Beijing: Science Press; p. 758–850. [Google Scholar]

