Evidence map›Paper›PMID 31682256›Full record

ArticleGigaScience2019

Chromosomal-level reference genome of Chinese peacock butterfly (Papilio bianor) based on third-generation DNA sequencing and Hi-C analysis.

Sihan Lu, Jie Yang, Xuelei Dai, Feiang Xie, Jinwu He, Zhiwei Dong, Junlai Mao, Guichun Liu, Zhou Chang, Ruoping Zhao and 5 more

Open access · goldAbstract read
In one paragraph

Article in GigaScience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

17 citing papers in PubMed, 55 citations in OpenAlex.

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  6. A polygenic explanation for Haldane's rule in butterflies.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  9. Frontiers in genetics · 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

15 authors at 5 institutions in 1 country.

Sihan LuCenter for Ecological and Environmental Sciences, Northwestern Polytechnical University, No.1 Dongxiang Road, Chang'an District, Xi'an, Shaanxi 710129, China.
Jie YangCenter for Ecological and Environmental Sciences, Northwestern Polytechnical University, No.1 Dongxiang Road, Chang'an District, Xi'an, Shaanxi 710129, China.
Xuelei DaiKey Laboratory of Animal Genetics, Breeding and Reproduction of Shaanxi Province, College of Animal Science and Technology, Northwest A&F University, No.22 Xinong Road,Yangling, Shaanxi 712100, China.
Feiang XieSchool of Marine Science and Technology, Zhejiang Ocean University, No.1 Haida South Road, Lincheng Changzhi Island, Zhoushan, Zhejiang 316022, China.
Jinwu HeCenter for Ecological and Environmental Sciences, Northwestern Polytechnical University, No.1 Dongxiang Road, Chang'an District, Xi'an, Shaanxi 710129, China.
Zhiwei DongState Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, No.32 Jiaochang Raod, Kunming, Yunnan 650223, China.
Junlai MaoSchool of Marine Science and Technology, Zhejiang Ocean University, No.1 Haida South Road, Lincheng Changzhi Island, Zhoushan, Zhejiang 316022, China.
Guichun LiuCenter for Ecological and Environmental Sciences, Northwestern Polytechnical University, No.1 Dongxiang Road, Chang'an District, Xi'an, Shaanxi 710129, China.
Zhou ChangState Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, No.32 Jiaochang Raod, Kunming, Yunnan 650223, China.
Ruoping ZhaoState Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, No.32 Jiaochang Raod, Kunming, Yunnan 650223, China.
Wenting WanCenter for Ecological and Environmental Sciences, Northwestern Polytechnical University, No.1 Dongxiang Road, Chang'an District, Xi'an, Shaanxi 710129, China.
Ru ZhangCenter for Ecological and Environmental Sciences, Northwestern Polytechnical University, No.1 Dongxiang Road, Chang'an District, Xi'an, Shaanxi 710129, China.
Yuan LiNextomics Biosciences Institute, No.666 Gaoxin Road, Wuhan, Hubei 430000, China.
Wen WangCenter for Ecological and Environmental Sciences, Northwestern Polytechnical University, No.1 Dongxiang Road, Chang'an District, Xi'an, Shaanxi 710129, China.
Xueyan LiState Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, No.32 Jiaochang Raod, Kunming, Yunnan 650223, China.
Northwestern Polytechnical University · CNKunming Institute of Zoology · CNZhejiang Ocean University · CNNextomics Biosciences (China) · CNNorth West Agriculture and Forestry University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPapilio bianor Cramer, 1777 (commonly known as the Chinese peacock butterfly) (Insecta, Lepidoptera, Papilionidae) is a widely distributed swallowtail butterfly with a wide number of geographic populations ranging from the southeast of Russia to China, Japan, India, Vietnam, Myanmar, and Thailand. Its wing color consists of both pigmentary colored scales (black, reddish) and structural colored scales (iridescent blue or green dust). A high-quality reference genome of P. bianor is an important foundation for investigating iridescent color evolution, phylogeography, and the evolution of swallowtail butterflies.

findingsWe obtained a chromosome-level de novo genome assembly of the highly heterozygous P. bianor using long Pacific Biosciences sequencing reads and high-throughput chromosome conformation capture technology. The final assembly is 421.52 Mb on 30 chromosomes (29 autosomes and 1 Z sex chromosome) with 13.12 Mb scaffold N50. In total, 15,375 protein-coding genes and 233.09 Mb of repetitive sequences were identified. Phylogenetic analyses indicated that P. bianor separated from a common ancestor of swallowtails ∼23.69-36.04 million years ago. Demographic history suggested that the population expansion of this species from the last interglacial period to the last glacial maximum possibly resulted from its decreased natural enemies and its adaptation to climate change during the glacial period.

conclusionsWe present a high-quality chromosome-level reference genome of P. bianor using long-read single-molecule sequencing and Hi-C-based chromatin interaction maps. Our results lay the foundation for exploring the genetic basis of special biological features of P. bianor and also provide a useful data source for comparative genomics and phylogenomics among butterflies and moths.

Indexed as

Genome, InsectHigh-Throughput Nucleotide SequencingPhylogenyAnimalsButterfliesChinaChromosome MappingChromosomes, Insectbutterflychromosome-level reference genomehigh-throughput chromosome conformation capture mapPapilio bianorsingle-molecule real-time (SMRT) sequencing

Identifiers

PMID31682256
PMCPMC6827417
OpenAlexW2983694693

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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.