Evidence map›Paper›PMID 33931033›Full record

ArticleBMC genomics2021

Comparative genomics of the coconut crab and other decapod crustaceans: exploring the molecular basis of terrestrial adaptation.

Werner Pieter Veldsman, Ka Yan Ma, Jerome Ho Lam Hui, Ting Fung Chan, J Antonio Baeza, Jing Qin, Ka Hou Chu

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 35 citations in OpenAlex.

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  10. Monosex Populations of the Giant Freshwater PrawnInternational journal of molecular sciences · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 4 countries.

Werner Pieter VeldsmanSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China. veldsman@link.cuhk.edu.hk.ORCID http://orcid.org/0000-0001-9837-8332
Ka Yan MaSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Jerome Ho Lam HuiSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Ting Fung ChanSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
J Antonio BaezaDepartment of Biological Sciences, Clemson University, 132 Long Hall, Clemson, SC, 29634, USA.
Jing QinSchool of Pharmaceutical Sciences (Shenzhen), Sun Yat-sen University, Shenzhen, China.
Ka Hou ChuSchool of Life Sciences, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China. kahouchu@cuhk.edu.hk.
Chinese University of Hong Kong · HKSun Yat-sen University · CNUniversidad Católica del Norte · CL

Funding

Hong Kong Research Grants Council C4042-14G
6 · The paper itself

Abstract

backgroundThe complex life cycle of the coconut crab, Birgus latro, begins when an obligate terrestrial adult female visits the intertidal to hatch zoea larvae into the surf. After drifting for several weeks in the ocean, the post-larval glaucothoes settle in the shallow subtidal zone, undergo metamorphosis, and the early juveniles then subsequently make their way to land where they undergo further physiological changes that prevent them from ever entering the sea again. Here, we sequenced, assembled and analyzed the coconut crab genome to shed light on its adaptation to terrestrial life. For comparison, we also assembled the genomes of the long-tailed marine-living ornate spiny lobster, Panulirus ornatus, and the short-tailed marine-living red king crab, Paralithodes camtschaticus. Our selection of the latter two organisms furthermore allowed us to explore parallel evolution of the crab-like form in anomurans.

resultsAll three assembled genomes are large, repeat-rich and AT-rich. Functional analysis reveals that the coconut crab has undergone proliferation of genes involved in the visual, respiratory, olfactory and cytoskeletal systems. Given that the coconut crab has atypical mitochondrial DNA compared to other anomurans, we argue that an abundance of kif22 and other significantly proliferated genes annotated with mitochondrial and microtubule functions, point to unique mechanisms involved in providing cellular energy via nuclear protein-coding genes supplementing mitochondrial and microtubule function. We furthermore detected in the coconut crab a significantly proliferated HOX gene, caudal, that has been associated with posterior development in Drosophila, but we could not definitively associate this gene with carcinization in the Anomura since it is also significantly proliferated in the ornate spiny lobster. However, a cuticle-associated coatomer gene, gammacop, that is significantly proliferated in the coconut crab, may play a role in hardening of the adult coconut crab abdomen in order to mitigate desiccation in terrestrial environments.

conclusionThe abundance of genomic features in the three assembled genomes serve as a source of hypotheses for future studies of anomuran environmental adaptations such as shell-utilization, perception of visual and olfactory cues in terrestrial environments, and cuticle sclerotization. We hypothesize that the coconut crab exhibits gene proliferation in lieu of alternative splicing as a terrestrial adaptation mechanism and propose life-stage transcriptomic assays to test this hypothesis.

Indexed as

AnomuraBrachyuraPalinuridaeAnimalsCocosFemaleGenomicsBirgus latroNuclear genomePanulirus ornatusParalithodes camtschaticus

Identifiers

PMID33931033
PMCPMC8086120
OpenAlexW3159562373

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.