Evidence map›Paper›PMID 35562825›Full record

ArticleBMC biology2022

Genome of a giant isopod, Bathynomus jamesi, provides insights into body size evolution and adaptation to deep-sea environment.

Jianbo Yuan, Xiaojun Zhang, Qi Kou, Yamin Sun, Chengzhang Liu, Shihao Li, Yang Yu, Chengsong Zhang, Songjun Jin, Jianhai Xiang and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 20 citations in OpenAlex.

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  7. The genome of the deep-sea anemoneProceedings. Biological sciences · 2023
    Article
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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

12 authors at 1 institution in 1 country.

Jianbo Yuan *CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Department of Marine Organism Taxonomy & Phylogeny, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.
Xiaojun Zhang *CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Department of Marine Organism Taxonomy & Phylogeny, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.
Qi Kou *CAS and Shandong Province Key Laboratory of Experimental Marine Biology, Department of Marine Organism Taxonomy & Phylogeny, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.
Yamin SunResearch Center for Functional Genomics and Biochip, Tianjin, 300457, China.
Chengzhang LiuCAS and Shandong Province Key Laboratory of Experimental Marine Biology, Department of Marine Organism Taxonomy & Phylogeny, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.
Shihao LiCAS and Shandong Province Key Laboratory of Experimental Marine Biology, Department of Marine Organism Taxonomy & Phylogeny, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.
Yang YuCAS and Shandong Province Key Laboratory of Experimental Marine Biology, Department of Marine Organism Taxonomy & Phylogeny, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.
Chengsong ZhangCAS and Shandong Province Key Laboratory of Experimental Marine Biology, Department of Marine Organism Taxonomy & Phylogeny, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.
Songjun JinCAS and Shandong Province Key Laboratory of Experimental Marine Biology, Department of Marine Organism Taxonomy & Phylogeny, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China.
Jianhai XiangCAS and Shandong Province Key Laboratory of Experimental Marine Biology, Department of Marine Organism Taxonomy & Phylogeny, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China. jhxiang@qdio.ac.cn.ORCID 0000-0001-5395-7787
Xinzheng LiCAS and Shandong Province Key Laboratory of Experimental Marine Biology, Department of Marine Organism Taxonomy & Phylogeny, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China. lixzh@qdio.ac.cn.
Fuhua LiCAS and Shandong Province Key Laboratory of Experimental Marine Biology, Department of Marine Organism Taxonomy & Phylogeny, Center for Ocean Mega-Science, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, 266071, China. fhli@qdio.ac.cn.ORCID 0000-0001-8693-600X
Institute of Oceanology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe deep-sea may be regarded as a hostile living environment, due to low temperature, high hydrostatic pressure, and limited food and light. Isopods, a species-rich group of crustaceans, are widely distributed across different environments including the deep sea and as such are a useful model for studying adaptation, migration, and speciation. Similar to other deep-sea organisms, giant isopods have larger body size than their shallow water relatives and have large stomachs and fat bodies presumably to store organic reserves. In order to shed light on the genetic basis of these large crustaceans adapting to the oligotrophic environment of deep-sea, the high-quality genome of a deep-sea giant isopod Bathynomus jamesi was sequenced and assembled.

resultsB. jamesi has a large genome of 5.89 Gb, representing the largest sequenced crustacean genome to date. Its large genome size is mainly attributable to the remarkable proliferation of transposable elements (84%), which may enable high genome plasticity for adaptive evolution. Unlike its relatives with small body size, B. jamesi has expanded gene families related to pathways of thyroid and insulin hormone signaling that potentially contribute to its large body size. Transcriptomic analysis showed that some expanded gene families related to glycolysis and vesicular transport were specifically expressed in its digestive organs. In addition, comparative genomics and gene expression analyses in six tissues suggested that B. jamesi has inefficient lipid degradation, low basal metabolic rate, and bulk food storage, suggesting giant isopods adopt a more efficient mechanism of nutrient absorption, storage, and utilization to provide sustained energy supply for their large body size.

conclusionsTaken together, the giant isopod genome may provide a valuable resource for understanding body size evolution and adaptation mechanisms of macrobenthic organisms to deep-sea environments.

Indexed as

IsopodaAdaptation, PhysiologicalAnimalsBody SizeGenomePhylogenyBody size evolutionDeep-seaGenome assemblyGiant isopodOligotrophic adaptation

Identifiers

PMID35562825
PMCPMC9107163
OpenAlexW4280504961

What OpenQuestion holds

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LicenceCC BY
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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.