Evidence map›Paper›PMID 26181055›Full record

ArticlePloS one2015

Identification of Laying-Related SNP Markers in Geese Using RAD Sequencing.

ShiGang Yu, WeiWei Chu, LiFan Zhang, HouMing Han, RongXue Zhao, Wei Wu, JiangNing Zhu, Michael V Dodson, Wei Wei, HongLin Liu and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

12 citing papers in PubMed, 30 citations in OpenAlex.

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  8. A Functional Mutation inInternational journal of molecular sciences · 2018
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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

11 authors at 2 institutions in 2 countries.

ShiGang YuCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, People's Republic of China.
WeiWei ChuCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, People's Republic of China.
LiFan ZhangCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, People's Republic of China.
HouMing HanJiangsu Lihua Animal Husbandry CO., LTD, Changzhou, People's Republic of China.
RongXue ZhaoJiangsu Lihua Animal Husbandry CO., LTD, Changzhou, People's Republic of China.
Wei WuJiangsu Lihua Animal Husbandry CO., LTD, Changzhou, People's Republic of China.
JiangNing ZhuJiangsu Lihua Animal Husbandry CO., LTD, Changzhou, People's Republic of China.
Michael V DodsonDepartment of Animal Sciences, Washington State University, Pullman, Washington, 99164, United States of America.
Wei WeiCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, People's Republic of China.
HongLin LiuCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, People's Republic of China.
Jie ChenCollege of Animal Science and Technology, Nanjing Agricultural University, Nanjing, People's Republic of China.
Nanjing Agricultural University · CNWashington State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Laying performance is an important economical trait of goose production. As laying performance is of low heritability, it is of significance to develop a marker-assisted selection (MAS) strategy for this trait. Definition of sequence variation related to the target trait is a prerequisite of quantitating MAS, but little is presently known about the goose genome, which greatly hinders the identification of genetic markers for the laying traits of geese. Recently developed restriction site-associated DNA (RAD) sequencing is a possible approach for discerning large-scale single nucleotide polymorphism (SNP) and reducing the complexity of a genome without having reference genomic information available. In the present study, we developed a pooled RAD sequencing strategy for detecting geese laying-related SNP. Two DNA pools were constructed, each consisting of equal amounts of genomic DNA from 10 individuals with either high estimated breeding value (HEBV) or low estimated breeding value (LEBV). A total of 139,013 SNP were obtained from 42,291,356 sequences, of which 18,771,943 were for LEBV and 23,519,413 were for HEBV cohorts. Fifty-five SNP which had different allelic frequencies in the two DNA pools were further validated by individual-based AS-PCR genotyping in the LEBV and HEBV cohorts. Ten out of 55 SNP exhibited distinct allele distributions in these two cohorts. These 10 SNP were further genotyped in a goose population of 492 geese to verify the association with egg numbers. The result showed that 8 of 10 SNP were associated with egg numbers. Additionally, liner regression analysis revealed that SNP Record-111407, 106975 and 112359 were involved in a multiplegene network affecting laying performance. We used IPCR to extend the unknown regions flanking the candidate RAD tags. The obtained sequences were subjected to BLAST to retrieve the orthologous genes in either ducks or chickens. Five novel genes were cloned for geese which harbored the candidate laying-related SNP, including membrane associated guanylate kinase (MAGI-1), KIAA1462, Rho GTPase activating protein 21 (ARHGAP21), acyl-CoA synthetase family member 2 (ACSF2), astrotactin 2 (ASTN2). Collectively, our data suggests that 8 SNP and 5 genes might be promising candidate markers or targets for marker-assisted selection of egg numbers in geese.

Indexed as

Polymorphism, Single NucleotideAnimalsFemaleGeeseGene FrequencyGenetic MarkersMolecular Sequence DataOviparitySequence Analysis, DNAGenetic Markers

Identifiers

PMID26181055
PMCPMC4504669
OpenAlexW923891776

What OpenQuestion holds

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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.