Evidence map›Paper›PMID 41157726›Full record

ArticlePlants (Basel, Switzerland)2025

Understanding Callus Types in Maize by Genetic Mapping and Transcriptional Profiling.

Guifang Lin, Yan Liu, Tej Man Tamang, Yang Qin, Mingxia Zhao, Jun Zheng, Guoying Wang, Hairong Wei, Sunghun Park, Myeong-Je Cho and 3 more

Abstract read
In one paragraph

Article in Plants (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Guifang LinDepartment of Plant Pathology, Kansas State University, Manhattan, KS 66506, USA.ORCID 0000-0002-4943-8607
Yan LiuState Key Laboratory of Crop Gene Resources and Breeding, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
Tej Man TamangDepartment of Plant Pathology, Kansas State University, Manhattan, KS 66506, USA.ORCID 0000-0003-0636-0376
Yang QinState Key Laboratory of Crop Gene Resources and Breeding, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, China.ORCID 0000-0001-9998-4713
Mingxia ZhaoDepartment of Plant Pathology, Kansas State University, Manhattan, KS 66506, USA.
Jun ZhengState Key Laboratory of Crop Gene Resources and Breeding, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, China.ORCID 0000-0002-3502-653X
Guoying WangState Key Laboratory of Crop Gene Resources and Breeding, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
Hairong WeiCollege of Forest Resources and Environmental Science, Michigan Technological University, Houghton, MI 49931, USA.ORCID 0000-0002-3551-4998
Sunghun ParkDepartment of Horticulture and Natural Resources, Kansas State University, Manhattan, KS 66506, USA.ORCID 0000-0003-1944-0463
Myeong-Je ChoInnovative Genomics Institute, University of California, Berkeley, CA 94704, USA.
Frank F WhiteDepartment of Plant Pathology, University of Florida, Gainesville, FL 32611, USA.ORCID 0000-0002-9905-2454
Yunjun LiuState Key Laboratory of Crop Gene Resources and Breeding, Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
Sanzhen LiuDepartment of Plant Pathology, Kansas State University, Manhattan, KS 66506, USA.ORCID 0000-0002-9513-855X

Funding

NSF 2011500NSF 2311738USDA 2021-67013-35724
6 · The paper itself

Abstract

Plant transformation efficiency is highly dependent on species, individual genotypes, and tissue types. In maize, immature embryos are regularly used for transformation. The process relies heavily on callus development, as it is intricately associated with somatic embryogenesis and subsequent plant regeneration, both of which directly affect transformation efficiency. Immature embryos of the segregation progeny derived from the two inbred parents, a transformation-amenable line A188 and a recalcitrant line B73, can be cultured to form two primary callus types: Type I and Type II. The Type II callus grows faster and is a favorable type for regeneration. Here, Type I and II calli from the B73xA188 F2 population were genotyped by Genotyping-By-Sequencing (GBS). Quantitative trait locus (QTL) analysis of the callus type identified QTLs at chromosomes 2, 5, 6, 8, and 9. The result was largely supported by the bulk segregant RNA-seq (BSR-seq) genetic analysis using RNA from separately pooled Type I and II calli. Both analyses revealed that an allele of A188 on chromosome 6 and B73 alleles on chromosomes 2, 5, 8, and 9 promoted the formation of the Type II callus. Differentially expressed genes (DEGs) between the Type II and I F2 calli were also identified. In addition, the A188 calli developed from the same immature embryos often exhibit heterogeneous morphology, including the fast- and slow-growing callus sectors. The transcriptional comparison between the two sectors was performed to identify DEGs. Both sets of DEGs were enriched in genes involved in cell-wall organization and wax biosynthesis pathways.

Indexed as

culturabilitymaizeplant transformationregeneration

Identifiers

PMID41157726
PMCPMC12566775

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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.