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File:Arapaima gigas 01.JPG Wikimedia Commons



File:Arapaima gigas 01.JPG  Wikimedia Commons
The particular Pirarucu (Arapaima gigas) is probably the world’s greatest freshwater fishes and member of typically the superorder Osteoglossomorpha (bonytongues), a single of the oldest lineages of ray-finned fishes. This species is an obligate air-breather found in typically the basin of the Amazon River with an attractive possible for aquaculture. Its phylogenetic position among bony these people own in makes the Pirarucu another subject for evolutionary research of early teleost diversity. Here, we present, initially, a draft genome version of the A. gigas genome, providing useful details for further functional and evolutionary studies. The A. gigas genome was assembled along with 103-Gb raw reads sequenced within an Illumina platform. The particular final draft genome set up was ∼661 Mb, with the contig N50 equal to fifty-one. 23 kb and scaffold N50 of 668 kb. Repeat sequences accounted for 21. 69% of the whole genome, and also a total of twenty-four, 655 protein-coding genes have been predicted from the genome assembly, by having an average of nine exons per gene. Phylogenomic analysis based upon 24 fish species supported the postulation that Osteoglossomorpha and Elopomorpha (eels, tarpons, and bonefishes) are cousin groups, both forming the sister lineage regarding Clupeocephala (remaining teleosts). Divergence period estimations suggested that Osteoglossomorpha and Elopomorpha lineages emerged independently in a amount of ∼30 Myr in typically the Jurassic. The draft genome of any. gigas provides a new valuable genetic resource regarding further investigations of evolutionary studies and may furthermore give a valuable data with regard to monetary applications.


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9 best Arapaima gigas images on Pinterest Freshwater fish, Fishing and Nature

Arapaima gigas, also known as Pirarucu or Paiche, is one of the world’s most significant freshwater fishes (Wijnstekers 2011) whose body length and weight may attain 4. 5 m (15 ft) and two hundred Kg (440 lb), respectively (Nelson 1994; Froese and Pauly 2018). The genus Arapaima emerged in the Amazon . com floodplain basin and will be presently distributed in Brazilian, Colombia, Ecuador, and Peru (Hrbek et al. 2006, 2007; Froese and Pauly 2018), and also within Thailand and Malaysia wherever it has been launched for commercial fishing (Froese and Pauly 2018). Arapaima gigas local name (Pirarucu) derives from your indigenous Tupi words “pira” and “urucum” for “fish” and “red, ” respectively, presumably referring to its red tail scales flecks or to the reddish flesh (Marsden year 1994; Godinho et al. 2005). The peculiarity from the inhaling and exhaling apparatus is characteristic of this Amazonian fish, including gills and a lung-like tissue devised for air-breathing produced from a modified in addition to enlarged swim bladder (Burnie and Wilson 2001; Brauner et al. 2004). Typically the Pirarucu has an appealing market value due to its low-fat and low bone content material. Overfishing practices inside the Amazonian region led to typically the banning of Pirarucu commercialization by the Brazilian government in 2001, although consumption by the native population is usually currently permitted under rigid size and seasoning rules (Bayley and Petrere 1989). Its main supply is provided by wild-caught fish and fish farming carried out by riverbank population of the Amazonas (Froese in addition to Pauly 2018). Aquaculture creation is attractive due to high carcass yields plus rapid juvenile growth, with yearlings reaching up to 10 kg (22 lb) (Almeida et al. 2013).
9 best Arapaima gigas images on Pinterest  Freshwater fish, Fishing and Nature



File:Arapaima Arapaima gigas 3.jpg Wikimedia Commons

Arapaima gigas belongs to the particular superorder Osteoglossomorpha of bony-tongued fishes whose tongue consists of sharp bony teeth regarding disabling and shredding preys (Sanford and Lauder 1990; Burnie and Wilson 2001). Combined with Elopomorpha (eels and tarpons) and Clupeocephala (most of extant fish species), the Osteoglossomorpha comprises 1 of the three main teleosts groups whose phylogenetic position has been controversial (Le et al. 1993; Inoue et al. 2003; Near et al. 2012; Betancur-R 2013; Faircloth et al. 2013; Chen et al. 2015; Hughes et al. 2018). Fossil information and some early molecular studies, including a recent comprehensive analysis of > 300 Actinopterygii species (Hughes et al. 2018), positioned Osteoglossomorpha since the oldest teleost group (Greenwood 1970; Inoue et al. 2003), whilst other studies located Elopomorpha as the most our ancestors one (Near et ing. 2012; Betancur-R 2013; Faircloth et al. 2013). Lately, a phylogenetic study according to whole genome sequencing of the bony-tongued Asian arowana (Scleropages formosus) suggested that the branching of Elopomorpha and Osteoglossomorpha occurred almost simultaneously, inserting them as sister lineages of Clupeocephala (Bian 2016). Within this framework, the genome of the Pirarucu provides new information to study the historical past of teleosts as properly as providing useful information for sustainable exploration associated with this giant Amazon fish. Here, we present the first whole genome assembly, gene annotation, and phylogenomic inference of the Pirarucu that ought to facilitate the molecular characterization and conservation regarding this economically important seafood species.
File:Arapaima Arapaima gigas 3.jpg  Wikimedia Commons


Arapaima Gigas

Test Collection and SequencingGenomic DNA was extracted through peripheral blood samples of four adult individuals (two males and two females) of Arapaima gigas: NCBI taxonomy ID 113544, FishBase ID: 2076. All samples were collected in accordance with the standards of the Federal University of Pará animal protocol. All of us applied a whole-genome shotgun sequencing strategy using a couple of short-insert libraries (400 in addition to 500 bp) in an Illumina HiSeq 2500 platform according in order to the manufacturer’s instructions (Illumina, San Diego, CA). HiSeq Rapid SBS Kits (FC-402-4021) and HiSeq Rapid Cluster Kits (PE-402-4002) were used to sequence paired-end read of 2 × 250 base sets. Read quality was examined using FastQC, version zero. 11. 4 (Andrews 2010), and low-quality reads had been trimmed with Sickle paired-end (pe), version 1. 33 (Joshi and Fass 2011), under default parameters.Genome Size Estimation and Sobre Novo AssemblageGenome dimension was estimated based about the k-mer spectrum using the following formula: G= (N×(L−K + 1)−B)/D. Where N is the particular total read count, D will be the read length, K is k-mer length (K = 31), B is the total low-frequency (frequency ≤1) k-mer count, D is the k-mer depth, and H is the genome size. Jellyfish 2. 2. 6th (Marçais and Kingsford 2011) was used to count number k-mer frequencies of high-quality sequencing reads.Genome assembly was performed using SOAPdenovo2 (version 2. 04) (Luo et al. 2012) beneath default parameters (127mer version). Three assemblies were performed: 1) using all reads; 2) with reads from male samples; and 3) with reads from women samples. Subsequently, gaps were filled using Redundants (Pryszcz and Gabaldón 2016) making use of three-run scaffolding steps: first of all with the default value associated with minimum read pairs to joining contigs (5 pairs), subsequently rerunning with prior data having a minimum worth of four read sets and, finally, utilizing a minimum of three read pairs. Assembly quality and data were assessed with QUAST (version 4. 4) (Gurevich et al. 2013).
Arapaima Gigas


THE FUCKING OCEAN YOU GUYS — Arapaima Gigas

Examination of Genome CompletenessAssemblage quality was measured by assessing gene completeness with Benchmarking Universal Single-Copy Orthologs (BUSCO) (Simão et 's. 2015) based on some, 584 BUSCO groups derived from Actinopterygii orthologs.Replicate AnalysisTransposable elements (TEs) and other repetitive factors of the Pirarucu genome were identified by a combined, homology-based method plus a de novo observation approach. Initially, tandem repeats were identified with Tandem Repeats Finder 4. 2009 (Benson 1999) with the following parameters: “Match=2, Mismatch=7, Delta=7, PM=80, PI=10, Minscore=50, and MaxPerid=2, 000. ” Additionally, a de novo repeat library was developed with RepeatModeler 1. zero. 9 and LTR_FINDER (Xu and Wang 2007), plus filtered with LTR_retriever (Ou and Jiang 2017) below default parameters. Subsequently, recognized and novel transposable components were identified by umschlüsselung the assembled sequences to the Repbase TE 22. 05 (Bao et al. 2015) and de novo do it again libraries using RepeatMasker some. 0 (Tarailo-Graovac and Chen 2009). In addition, all of us annotated TE-related proteins making use of RepeatProteinMask 4. 0 (Tarailo-Graovac and Chen 2009).Gene Structure and Function AnnotationGenome annotation was performed with the MAKER2 pipeline (Holt and Yandell 2011) inside a two-pass iteration. First, homology annotation was performed with protein data through Homo sapiens (human), Danio rerio (zebrafish), Takifugu rubripes (Japanese fugu), Tetraodon nigroviridis (spotted green pufferfish), Gasterosteus aculeatus (three-spined stickleback), Oryzias latipes (Japanese medaka), Latimeria chalumnae (coelacanth) (Ensembl launch 88), together with Scleropages formosus (Asian arowana) protein sequences from NCBI RefSeq annotation data. Subsequently, sobre novo annotations were carried out using the homology-based outcomes achieved in the 1st step. We also used the RepeatModeller 1. 0. 9 (Smit and Hubley 2008) to build a de novo repeat library with default parameters. The GFF output from the 1st step was used to train the SNAP 20131129 (Korf 2004) and AUGUSTUS 3. 2. 3 (Stanke et al. 2008) predictors. GeneMark-ES 4. 32 (Lomsadze et al. 2005) was trained using the genome assembly itself. InterProScan 5. 24-63. 0 (Jones et al. 2014) was operate on the protein output associated with MAKER, providing gene ontologies and classifying protein domain names and families. Protein result was compared using GREAT TIME against the NCBI NR database (available on Might 29, 2017) for identifying putative gene names. Blast2GO v5 (Conesa et 's. 2005) was subsequently utilized to obtain Gene Ontology mapping and annotation (supplementary file S2, Supplementary Material online).
THE FUCKING OCEAN YOU GUYS — Arapaima Gigas



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