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 PMID:29874592  

High-Quality Genome Assemblies Reveal Long Non-coding RNAs Expressed in Ant Brains.

Emily J Shields | Lihong Sheng | Amber K Weiner | Benjamin A Garcia | Roberto Bonasio
Cell reports | 2018

Ants are an emerging model system for neuroepigenetics, as embryos with virtually identical genomes develop into different adult castes that display diverse physiology, morphology, and behavior. Although a number of ant genomes have been sequenced to date, their draft quality is an obstacle to sophisticated analyses of epigenetic gene regulation. We reassembled de novo high-quality genomes for two ant species, Camponotus floridanus and Harpegnathos saltator. Using long reads enabled us to span large repetitive regions and improve genome contiguity, leading to comprehensive and accurate protein-coding annotations that facilitated the identification of a Gp-9-like gene as differentially expressed in Harpegnathos castes. The new assemblies also enabled us to annotate long non-coding RNAs in ants, revealing caste-, brain-, and developmental-stage-specific long non-coding RNAs (lncRNAs) in Harpegnathos. These upgraded genomes, along with the new gene annotations, will aid future efforts to identify epigenetic mechanisms of phenotypic and behavioral plasticity in ants.

Pubmed ID: 29874592

Research resources used in this publication

None found

Additional research tools detected in this publication

Antibodies used in this publication

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Associated grants

  • Agency: NIMH NIH HHS, United States
    Id: DP2 MH107055
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM110174
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL122993
  • Agency: NHGRI NIH HHS, United States
    Id: T32 HG000046

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This is a list of tools and resources that we have found mentioned in this publication.


Pilon (tool)

RRID:SCR_014731

Software tool to automatically improve draft assemblies and find variation among strains, including large event detection. FASTA files of genome along with one or more BAM files of reads aligned as input. Read alignment analysis is used to identify inconsistencies between input genome and evidence in reads, then attempts to make improvements to genome.

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Canu (tool)

RRID:SCR_015880

Software for scalable and accurate long-read assembly via adaptive k-mer weighting and repeat separation. Canu is a fork of the Celera Assembler and is designed for high-noise single-molecule sequencing (such as the PacBio RS II/Sequel or Oxford Nanopore MinION).

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