Posted By:

Giant Arapaima Arapaima gigas ZooChat



Giant Arapaima Arapaima gigas  ZooChat
The particular Pirarucu (Arapaima gigas) is probably the world’s most significant freshwater fish and member of the particular superorder Osteoglossomorpha (bonytongues), one of the oldest lineages of ray-finned fishes. This specific species is an obligate air-breather found in the basin of the Amazon online River with an attractive potential for aquaculture. Its phylogenetic position among bony fish makes the Pirarucu a relevant subject for evolutionary scientific studies of early teleost variation. Here, we present, the first time, a draft genome edition of the A. gigas genome, providing useful information for further functional and major studies. The A. gigas genome was assembled along with 103-Gb raw reads sequenced within an Illumina platform. The particular final draft genome assemblage 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 a total of twenty four, 655 protein-coding genes had been predicted from the genome assembly, with an average of nine exons per gene. Phylogenomic analysis based about 24 fish species reinforced the postulation that Osteoglossomorpha and Elopomorpha (eels, tarpons, and bonefishes) are sibling groups, both forming the sister lineage with respect to Clupeocephala (remaining teleosts). Divergence period estimations suggested that Osteoglossomorpha and Elopomorpha lineages surfaced independently in a amount of ∼30 Myr in the Jurassic. The draft genome of any. gigas provides a valuable genetic resource for further investigations of major studies and may likewise give a valuable data regarding economical applications.


Rangking: 20

Size: 951.4KB

Width: 1600

Height: 966




Big Fishes of the World: ARAPAIMA PIRARUCU Arapaima gigas

Arapaima gigas, also known as Pirarucu or Paiche, is 1 of the world’s greatest freshwater fishes (Wijnstekers 2011) whose body length in addition to weight may attain four. 5 m (15 ft) and 200 Kg (440 lb), respectively (Nelson 1994; Froese and Pauly 2018). The genus Arapaima emerged in the Amazon floodplain basin and will be presently distributed in Brazil, Colombia, Ecuador, and Peru (Hrbek et al. june 2006, 2007; Froese and Pauly 2018), and also in Thailand and Malaysia where it has been introduced 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 mentioning to its red tail scales flecks or its reddish flesh (Marsden 1994; Godinho et al. 2005). The peculiarity from the inhaling and exhaling apparatus is characteristic regarding this Amazonian fish, comprising gills and a lung-like tissue devised for air-breathing derived from a modified plus enlarged swim bladder (Burnie and Wilson 2001; Brauner et al. 2004). Typically the Pirarucu has an appealing market value due to its less fat and low bone content material. Overfishing practices inside the Amazonian region led to the banning of Pirarucu commercialization by the Brazilian authorities in 2001, although consumption with 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 species of fish and fish farming carried out by riverbank population of the Amazonas (Froese in addition to Pauly 2018). Aquaculture production is attractive due to high carcass yields plus rapid juvenile growth, together with yearlings reaching up to 10 kg (22 lb) (Almeida et al. 2013).
Big Fishes of the World: ARAPAIMA  PIRARUCU Arapaima gigas



Osteoglossomorpha Wikipedia

Arapaima gigas belongs to the particular superorder Osteoglossomorpha of bony-tongued fishes whose tongue consists of sharp bony teeth with regard to disabling and shredding preys (Sanford and Lauder 1990; Burnie and Wilson 2001). Along with Elopomorpha (eels in addition to tarpons) and Clupeocephala (most of extant fish species), the Osteoglossomorpha comprises 1 of the three main teleosts groups whose phylogenetic position has been debatable (Le et al. 1993; Inoue et al. 2003; Near et al. 2012; Betancur-R 2013; Faircloth ainsi que al. 2013; Chen et al. 2015; Hughes et al. 2018). Fossil information and some early molecular studies, including a latest comprehensive analysis of > 300 Actinopterygii species (Hughes et al. 2018), positioned Osteoglossomorpha because the oldest teleost group (Greenwood 1970; Inoue et al. 2003), although 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 typically the branching of Elopomorpha and Osteoglossomorpha occurred almost simultaneously, inserting them as sister lineages of Clupeocephala (Bian 2016). Within this circumstance, the genome of the Pirarucu provides new information to study the historical past of teleosts as properly as providing useful details for sustainable exploration regarding this giant Amazon fish. Here, we present the particular first whole genome assembly, gene annotation, and phylogenomic inference of the Pirarucu which should facilitate the molecular characterization and conservation of this economically important seafood species.
Osteoglossomorpha  Wikipedia


Arapaima gigas Merifish Aquariums.

Test Collection and SequencingGenomic DNA was extracted through peripheral blood samples associated with four adult individuals (two males and two females) of Arapaima gigas: NCBI taxonomy ID 113544, FishBase ID: 2076. All examples were collected in agreement with the standards associated with the Federal University regarding Pará animal protocol. We applied a whole-genome shotgun sequencing strategy using two short-insert libraries (400 in addition to 500 bp) in a Illumina HiSeq 2500 platform according to the manufacturer’s instructions (Illumina, San Diego, CA). HiSeq Rapid SBS Kits (FC-402-4021) and HiSeq Rapid Bunch Kits (PE-402-4002) were utilized 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 have been trimmed with Sickle paired-end (pe), version 1. 33 (Joshi and Fass 2011), under default parameters.Genome Size Estimation and Sobre Novo AssemblageGenome size was estimated based on the k-mer spectrum using the following formula: G= (N×(L−K + 1)−B)/D. Where N is typically the total read count, D will be the read length, K is k-mer length (K = 31), B is the overall low-frequency (frequency ≤1) k-mer count, D is the particular k-mer depth, and Gary the gadget guy is the genome dimension. Jellyfish 2. 2. six (Marçais and Kingsford 2011) was used to depend k-mer frequencies of high-quality sequencing reads.Genome set up was performed using SOAPdenovo2 (version 2. 04) (Luo et al. 2012) under default parameters (127mer version). Three assemblies were performed: 1) using all reads; 2) with reads coming 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 all the default value of minimum read pairs in order to joining contigs (5 pairs), subsequently rerunning with previous data with a minimum benefit of four read sets and, finally, utilizing a lowest of three read pairs. Assembly quality and stats were assessed with QUAST (version 4. 4) (Gurevich et al. 2013).
Arapaima gigas  Merifish Aquariums.


Arapaima gigas 120 kg ,Amazonie YouTube

Examination of Genome CompletenessAssemblage quality was measured simply by assessing gene completeness along with Benchmarking Universal Single-Copy Orthologs (BUSCO) (Simão et ing. 2015) based on four, 584 BUSCO groups derived from Actinopterygii orthologs.Do it again AnalysisTransposable elements (TEs) and other repetitive factors of the Pirarucu genome were identified by the combined, homology-based method in addition to a de novo annotation approach. Initially, tandem repeats were identified with Conjunction Repeats Finder 4. 09 (Benson 1999) with the particular 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), and filtered with LTR_retriever (Ou and Jiang 2017) beneath default parameters. Subsequently, known and novel transposable factors were identified by mapping the assembled sequences for 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, we annotated TE-related proteins applying RepeatProteinMask 4. 0 (Tarailo-Graovac and Chen 2009).Gene Structure and Function ObservationGenome annotation was performed with the MAKER2 pipeline (Holt and Yandell 2011) inside a two-pass iteration. Very first, homology annotation was performed with protein data from 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 release 88), together with Scleropages formosus (Asian arowana) proteins sequences from NCBI RefSeq annotation data. Subsequently, sobre novo annotations were performed using the homology-based outcomes achieved in the 1st step. We also used the RepeatModeller 1. 0. nine (Smit and Hubley 2008) to build a sobre novo repeat library along with default parameters. The GFF output from the very first step was used in order 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 five. 24-63. 0 (Jones ainsi que al. 2014) was operate on the protein output associated with MAKER, providing gene ontologies and classifying protein domain names and families. Protein output was compared using BLAST against the NCBI NR database (available on Might 29, 2017) for identifying putative gene names. Blast2GO v5 (Conesa et al. 2005) was subsequently used to obtain Gene Ontology mapping and annotation (supplementary file S2, Supplementary Materials online).
Arapaima gigas 120 kg ,Amazonie  YouTube



IKLAN BODY

0 Komentar