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Mitogenome Announcement

The complete mitogenome of the rockweed Fucus distichus (Fucaceae, Phaeophyceae)

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Pages 203-204 | Received 07 Mar 2017, Accepted 21 Mar 2017, Published online: 07 Apr 2017

Abstract

The rockweed F. distichus is a one of the most common intertidal seaweeds in the northern hemisphere. The systematics of F. distichus however remains open to discussion. Here, we contribute to the bioinformatics and systematics of F. distichus by deciphering its complete mitogenome. The F. distichus mitogenome is 36,400 bp in length, contains 67 genes, and has a gene content, organization, and sequence that are similar to the generitype, F. vesiculusus. These data support the continued recognition of F. distichus as a polymorphic entity with a broad distribution and high degree of ecological diversity.

Fucus L. is one of the three original genera proposed by Linnaeus (Citation1753) to accommodate macroscopic marine algae. Since then more than 1000 names have been assigned to the genus (Guiry & Guiry Citation2017), but nearly all have been reclassified. Based on genetic analyses, three or four species are recognized: F. distichus L., F. serratus L., F. spiralis L., and F. vesiculosus L. (Serrao et al. Citation1999; Coyer et al. Citation2006; Kucera & Saunders Citation2008; Coyer et al. Citation2011; Laughinghouse et al. Citation2015). This classification remains problematic however, as exemplified by F. distichus, which displays a high degree of morphological, ecological, geographical, and reproductive variation (Gardner Citation1922; Kucera & Saunders Citation2008; Coyer et al. Citation2011; Laughinghouse et al. Citation2015). Herein, we characterize the mitogenome of F. distichus to clarify its systematics.

Fucus distichus (Voucher- UC 2050487) was collected from Coos Bay, Oregon (43°21′30.3″, −124°18′32.2″) and its DNA isolated following Lindstrom et al. (Citation2011). The 76 bp paired-end library construction and sequencing was performed by myGenomics, LLC (Alpharetta, GA,) yielding 22,040,820 reads. The mitogenome was assembled using the default de novo settings in CLC Genomics Workbench 9.5 (®2016 CLC bio, a QIAGEN Company, Waltham, MA) and annotated using blastx and NCBI ORF-finder. The mitogenome was aligned to other Phaeophyceae with MAFFT (Katoh & Standley Citation2013). The RaxML analysis was executed using complete mitogenome sequences at Trex-online (Boc & Makarenkov Citation2012) with the GTR + gamma model and 1000 fast bootstraps, then visualized with TreeDyn 198.3 at Phylogeny.fr (Dereeper et al. Citation2008).

The F. distichus mitogenome (GenBank KY678904) is 36,400 bp in length and contains cob and tatC, 3 rRNA, 3 open reading frames, 3 ATP synthase, 3 cox, 6 rpl, 10 NADH, 11 rps, and 26 tRNA genes (trnL occurs in triplicate and trnI, trnM, trnS, trnY in duplicate). Gene content, organization, and length are nearly identical to F. vesiculosus (36,392 bp) (Oudot-Le Secq et al. Citation2006). The genetic distance between these two species is 2.0%. Phylogenetic analysis of F. distichus supports this close relationship, positioning it in a clade with F. vesiculosus (). Sequence analysis of F. distichus from Oregon identifies it as haplotype ic6 (Coyer et al. Citation2011) from Japan and Alaska, USA. Its cox1 sequence was also an exact match to a specimen from British Columbia, Canada (GenBank EU646633), and only differed by 1 bp from F. distichus from Nova Scotia, Canada (GenBank EU646647), Nordland, Norway (GenBank LN877838), and California, USA (GenBank KM254965).

Figure 1. Maximum-likelihood phylogram of F. distichus (bold letters) and related Phaeophyceae mitogenomes. Numbers along branches are RaxML bootstrap supports based on 1000 nreps. The legend below represents the scale for nucleotide substitutions.

Figure 1. Maximum-likelihood phylogram of F. distichus (bold letters) and related Phaeophyceae mitogenomes. Numbers along branches are RaxML bootstrap supports based on 1000 nreps. The legend below represents the scale for nucleotide substitutions.

Disclosure statement

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.

Additional information

Funding

This work was made possible by a private family trust from Paul W. Gabrielson.

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