Evidence map›Paper›PMID 30743052›Full record

ArticleGenomics, proteomics & bioinformatics2018

An Exome-seq Based Tool for Mapping and Selection of Candidate Genes in Maize Deletion Mutants.

Shangang Jia, Kyla Morton, Chi Zhang, David Holding

Abstract read
In one paragraph

Article in Genomics, proteomics & bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Shangang JiaDepartment of Agronomy and Horticulture, Center for Plant Science Innovation, Beadle Center for Biotechnology, University of Nebraska, Lincoln, NE 68588, USA.
Kyla MortonDepartment of Agronomy and Horticulture, Center for Plant Science Innovation, Beadle Center for Biotechnology, University of Nebraska, Lincoln, NE 68588, USA.
Chi ZhangSchool of Biological Sciences, Center for Plant Science Innovation, Beadle Center for Biotechnology, University of Nebraska, Lincoln, NE 68588, USA.
David HoldingDepartment of Agronomy and Horticulture, Center for Plant Science Innovation, Beadle Center for Biotechnology, University of Nebraska, Lincoln, NE 68588, USA. Electronic address: dholding2@unl.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the large number of genomic and transcriptomic resources in maize, there is still much to learn about the function of genes in developmental and biochemical processes. Some maize mutants that were generated by gamma-irradiation showed clear segregation for the kernel phenotypes in B73 × Mo17 F2 ears. To better understand the functional genomics of kernel development, we developed a mapping and gene identification pipeline, bulked segregant exome sequencing (BSEx-seq), to map mutants with kernel phenotypes including opaque endosperm and reduced kernel size. BSEx-seq generates and compares the sequence of the exon fraction from mutant and normal plant F2 DNA pools. The comparison can derive mapping peaks, identify deletions within the mapping peak, and suggest candidate genes within the deleted regions. We then used the public kernel-specific expression data to narrow down the list of candidate genes/mutations and identified deletions ranging from several kb to more than 1 Mb. A full deletion allele of the Opaque-2 gene was identified in mutant 531, which occurs within a ∼200-kb deletion. Opaque mutant 1486 has a 6248-bp deletion in the mapping interval containing two candidate genes encoding RNA-directed DNA methylation 4 (RdDM4) and AMP-binding protein, respectively. This study demonstrates the efficiency and cost-effectiveness of BSEx-seq for causal mutation mapping and candidate gene selection, providing a new option in mapping-by-sequencing for maize functional genomics studies.

Indexed as

Gene DeletionChromosome MappingDNA-Binding ProteinsDNA, PlantEndospermExomeExonsGenomicsPhenotypePlant ProteinsSequence Analysis, DNATranscription FactorsZea maysDNA-Binding ProteinsDNA, Plantopaque-2 protein, Zea maysPlant ProteinsTranscription FactorsBulked segregation analysisExome-seqMaize functional genomicsMapping-by-sequencingOpaque mutant

Identifiers

PMID30743052
PMCPMC6411947

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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.