4.7 Article

An Updated Genome Assembly Improves Understanding of the Transcriptional Regulation of Coloration in Midas Cichlid

期刊

FRONTIERS IN MARINE SCIENCE
卷 9, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fmars.2022.950573

关键词

Midas cichlid; morphological polymorphism; high-quality genome; melanin; transcriptome

资金

  1. Open Fund of Key Laboratory of Recreational Fisheries, China Ministry of Agriculture and Rural Areas
  2. Neijiang Normal University Innovation Team Fund [2019N01]
  3. Guangdong Provincial Special Fund for Modern Agriculture Industry Technology Innovation Team [2021TD03]
  4. National Freshwater Genetic Resource Center [2022KJ150]
  5. [FGRC18537]

向作者/读者索取更多资源

This study generated a high-quality genome assembly and gene annotation of Midas cichlid, providing a valuable genetic resource for biological studies on this species. Through comparisons between dark and gold individuals, differential expressional genes and key functional modules were identified, enhancing our understanding of the transcriptional regulatory mechanisms underlying coloration changes. This research is of great importance not only for Midas cichlid, but also for other fish species in freshwater to marine ecosystems.
Midas cichlid (Amphilophus citrinellus), a popular aquarium fish, attracts extensive attention from worldwide biologists mainly due to its morphological polymorphism (dark versus gold). Continuous efforts have therefore been paid to address mechanisms of its coloration variants, while it is far away from the detailed illustration of a clear regulatory network. Some limits may come from the absence of a high-quality genome assembly and a relatively accurate gene set. In this study, we sequenced about 149 Gb of nucleotide sequences of Midas cichlid, generating a genome assembly with a total size of 933.5 Mb, which exhibits a good genome continuity with a contig N50 of 10.5 Mb. A total of 25,911 protein-coding genes were annotated and about 90% completeness was achieved, which helps to build a good gene pool for understanding expressional differences of color variation. With the assistance of the final gene set, we identified a total of 277 differential expressional genes (DEGs), of which 97 up- and 180 downregulated were determined in dark-vs-gold comparisons. Two protein-protein interaction (PPI) networks were constructed from these DEGs, and three key functional modules were classified. Hub genes within each module were evaluated, and we found that the third key module contains tyrp1b, oca2, pmela, tyr, and slc24a5, which were previously proven to be associated with melanin formation. Two downregulated DEGs (myl1 and pgam2) in the first key module may be involved in muscle movement and spermatogenesis, implying that certain side effects could result from the morphological polymorphism. The first key module, consisting of proteins encoded by upregulated DEGs that were associated with MAPK signaling, Toll-like receptor signaling, and gonadotropin-releasing hormone pathways, may contribute to a negative upstream regulation or downstream influence on melanin biosynthesis. Taken together, our new genome assembly and gene annotation of Midas cichlid provide a high-quality genetic resource for biological studies on this species, and the newly identified key networks and hub genes in dark-vs-gold comparisons enhance our understanding of the transcriptional regulatory mechanisms underlying coloration changes not only in Midas cichlid but also in other fishes from freshwater to marine ecosystems.

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