4.3 Article

Genome of the Rio Pearlfish (Nematolebias whitei), a bi-annual killifish model for Eco-Evo-Devo in extreme environments

Journal

G3-GENES GENOMES GENETICS
Volume 12, Issue 4, Pages -

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/g3journal/jkac045

Keywords

Nematolebias whitei; Rio Pearlfish; diapause; aging; hatching; extreme environments; Eco-Evo-Devo; teleost

Funding

  1. National Science Foundation Bio/computational Evolution in Action CONsortium grant (NSF BEACON) [DBI-0939454, 1233]
  2. National Institutes of Health Office of Research Infrastructure Programs [NIH ORIP R01OD011116]

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The Rio Pearlfish is a killifish species that inhabits seasonal pools in the Rio de Janeiro region of Brazil. Its embryos enter dormant diapause stages in the soil and hatch when the habitat is inundated. The genome of the Rio Pearlfish provides important insights into the genetic control of hatching and the adaptation to harsh conditions.
The Rio Pearlfish, Nematolebias whitei, is a bi-annual killifish species inhabiting seasonal pools in the Rio de Janeiro region of Brazil that dry twice per year. Embryos enter dormant diapause stages in the soil, waiting for the inundation of the habitat which triggers hatching and commencement of a new life cycle. Rio Pearlfish represents a convergent, independent origin of annualism from other emerging killifish model species. While some transcriptomic datasets are available for Rio Pearlfish, thus far, a sequenced genome has been unavailable. Here, we present a high quality, 1.2 Gb chromosome-level genome assembly, genome annotations, and a comparative genomic investigation of the Rio Pearlfish as representative of a vertebrate clade that evolved environmentally cued hatching. We show conservation of 3D genome structure across teleost fish evolution, developmental stages, tissues, and cell types. Our analysis of mobile DNA shows that Rio Pearlfish, like other annual killifishes, possesses an expanded transposable element profile with implications for rapid aging and adaptation to harsh conditions. We use the Rio Pearlfish genome to identify its hatching enzyme gene repertoire and the location of the hatching gland, a key first step in understanding the developmental genetic control of hatching. The Rio Pearlfish genome expands the comparative genomic toolkit available to study convergent origins of seasonal life histories, diapause, and rapid aging phenotypes. We present the first set of genomic resources for this emerging model organism, critical for future functional genetic, and multiomic explorations of Eco-Evo-Devo phenotypes of resilience and adaptation to extreme environments.

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