Evidence map›Paper›PMID 24359812›Full record

ArticleGenome biology2013

Obligate mutualism within a host drives the extreme specialization of a fig wasp genome.

Jin-Hua Xiao, Zhen Yue, Ling-Yi Jia, Xin-Hua Yang, Li-Hua Niu, Zhuo Wang, Peng Zhang, Bao-Fa Sun, Shun-Min He, Zi Li and 42 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
13.3field-weighted citation impact, top 1% 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

49 citing papers in PubMed, 104 citations in OpenAlex.

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  10. Genomic signatures associated with the evolutionary loss of egg yolk in parasitoid wasps.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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

52 authors at 13 institutions in 4 countries.

Jin-Hua Xiao
Zhen Yue
Ling-Yi Jia
Xin-Hua Yang
Li-Hua Niu
Zhuo Wang
Peng Zhang
Bao-Fa Sun
Shun-Min He
Zi Li
Tuan-Lin Xiong
Wen Xin
Hai-Feng Gu
Bo Wang
John H Werren
Robert W Murphy
David Wheeler
Li-Ming Niu
Guang-Chang Ma
Ting Tang
Sheng-Nan Bian
Ning-Xin Wang
Chun-Yan Yang
Nan Wang
Yue-Guan Fu
Wen-Zhu Li
Soojin V Yi
Xing-Yu Yang
Qing Zhou
Chang-Xin Lu
Chun-Yan Xu
Li-Juan He
Li-Li Yu
Ming Chen
Yuan Zheng
Shao-Wei Wang
Shuang Zhao
Yan-Hong Li
Yang-Yang Yu
Xiao-Ju Qian
Yue Cai
Lian-Le Bian
Shu Zhang
Jun-Yi Wang
Ye Yin
Hui Xiao
Guan-Hong Wang
Hui Yu
Wen-Shan Wu
James M Cook
Jun Wang
Da-Wei Huang
BGI Group (China) · CNChinese Academy of Sciences · CNChinese Academy of Tropical Agricultural Sciences · CNShandong Agricultural University · CNHebei University · CNUniversity of Chinese Academy of Sciences · CNUniversity of Rochester · USBeijing Botanical Garden · CNFujian Normal University · CNGeorgia Institute of Technology · USKunming Institute of Zoology · CNSinovac Biotech · CNUniversity of Reading · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFig pollinating wasps form obligate symbioses with their fig hosts. This mutualism arose approximately 75 million years ago. Unlike many other intimate symbioses, which involve vertical transmission of symbionts to host offspring, female fig wasps fly great distances to transfer horizontally between hosts. In contrast, male wasps are wingless and cannot disperse. Symbionts that keep intimate contact with their hosts often show genome reduction, but it is not clear if the wide dispersal of female fig wasps will counteract this general tendency. We sequenced the genome of the fig wasp Ceratosolen solmsi to address this question.

resultsThe genome size of the fig wasp C. solmsi is typical of insects, but has undergone dramatic reductions of gene families involved in environmental sensing and detoxification. The streamlined chemosensory ability reflects the overwhelming importance of females finding trees of their only host species, Ficus hispida, during their fleeting adult lives. Despite long-distance dispersal, little need exists for detoxification or environmental protection because fig wasps spend nearly all of their lives inside a largely benign host. Analyses of transcriptomes in females and males at four key life stages reveal that the extreme anatomical sexual dimorphism of fig wasps may result from a strong bias in sex-differential gene expression.

conclusionsOur comparison of the C. solmsi genome with other insects provides new insights into the evolution of obligate mutualism. The draft genome of the fig wasp, and transcriptomic comparisons between both sexes at four different life stages, provide insights into the molecular basis for the extreme anatomical sexual dimorphism of this species.

Indexed as

Genome, InsectAnimalsEvolution, MolecularFemaleFicusGene Expression Regulation, DevelopmentalGenome SizeMalePhylogenySequence Analysis, DNASex CharacteristicsSymbiosisWasps

Identifiers

PMID24359812
PMCPMC4053974
OpenAlexW2110793265

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.