Evidence map›Paper›PMID 27354512›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Analysis of tandem gene copies in maize chromosomal regions reconstructed from long sequence reads.

Jiaqiang Dong, Yaping Feng, Dibyendu Kumar, Wei Zhang, Tingting Zhu, Ming-Cheng Luo, Joachim Messing

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
22.6field-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

27 citing papers in PubMed, 44 citations in OpenAlex.

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  7. Genomics-Enabled Analysis ofInternational journal of molecular sciences · 2020
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  8. Plant evolution and environmental adaptation unveiled by long-read whole-genome sequencing ofProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  9. Article
  10. NAC-type transcription factors regulate accumulation of starch and protein in maize seeds.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  11. High frequency DNA rearrangement atCommunications biology · 2019
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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 2 institutions in 1 country.

Jiaqiang DongWaksman Institute of Microbiology, Rutgers, The State University of New Jersey, Piscataway, NJ 08854;
Yaping FengWaksman Institute of Microbiology, Rutgers, The State University of New Jersey, Piscataway, NJ 08854;
Dibyendu KumarWaksman Institute of Microbiology, Rutgers, The State University of New Jersey, Piscataway, NJ 08854;
Wei ZhangWaksman Institute of Microbiology, Rutgers, The State University of New Jersey, Piscataway, NJ 08854;
Tingting ZhuDepartment of Plant Sciences, University of California, Davis, CA 95616.
Ming-Cheng LuoDepartment of Plant Sciences, University of California, Davis, CA 95616.
Joachim MessingWaksman Institute of Microbiology, Rutgers, The State University of New Jersey, Piscataway, NJ 08854; messing@waksman.rutgers.edu.
Rutgers, The State University of New Jersey · USUniversity of California, Davis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Haplotype variation not only involves SNPs but also insertions and deletions, in particular gene copy number variations. However, comparisons of individual genomes have been difficult because traditional sequencing methods give too short reads to unambiguously reconstruct chromosomal regions containing repetitive DNA sequences. An example of such a case is the protein gene family in maize that acts as a sink for reduced nitrogen in the seed. Previously, 41-48 gene copies of the alpha zein gene family that spread over six loci spanning between 30- and 500-kb chromosomal regions have been described in two Iowa Stiff Stalk (SS) inbreds. Analyses of those regions were possible because of overlapping BAC clones, generated by an expensive and labor-intensive approach. Here we used single-molecule real-time (Pacific Biosciences) shotgun sequencing to assemble the six chromosomal regions from the Non-Stiff Stalk maize inbred W22 from a single DNA sequence dataset. To validate the reconstructed regions, we developed an optical map (BioNano genome map; BioNano Genomics) of W22 and found agreement between the two datasets. Using the sequences of full-length cDNAs from W22, we found that the error rate of PacBio sequencing seemed to be less than 0.1% after autocorrection and assembly. Expressed genes, some with premature stop codons, are interspersed with nonexpressed genes, giving rise to genotype-specific expression differences. Alignment of these regions with those from the previous analyzed regions of SS lines exhibits in part dramatic differences between these two heterotic groups.

Indexed as

Gene DosageGenes, PlantDNA, PlantGenome, PlantHaplotypesSequence Analysis, DNAZea maysDNA, Plantgene copy numberhaplotype variationmaize genomeshotgun DNA sequencingtransposable elements

Identifiers

PMID27354512
PMCPMC4961126
OpenAlexW2460883242

What OpenQuestion holds

Textmetadata
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.