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SRX18249874: GSM6730007: RHW1-crispr-rep2; Zea mays; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 26.9M spots, 8.1G bases, 2.4Gb downloads

External Id: GSM6730007_r1
Submitted by: Yan He Lab, Plant Genetics and Breeding, China Agricultural University
Study: The RHW1-ZCN4 regulatory pathway confers natural variation of husk leaf width in maize
show Abstracthide Abstract
Maize husk leaf - the outer leafy layers covering the ear - modulates kernel yield and quality. Despite its importance, however, the genetic controls underlying husk leaf development remain elusive. Our previous genome-wide association study identified a single nucleotide polymorphism located in the gene RHW1 (Regulator of Husk leaf Width) that is significantly associated with husk leaf-width diversity in maize. Here, we further demonstrate that a polymorphic 18-bp InDel (insertion/deletion) variant in the 3' untranslated region of RHW1 alters its protein abundance and accounts for husk leaf width variation. RHW1 encodes a putative MYB-like transcriptional repressor. Disruption of RHW1 altered cell proliferation and resulted in a narrower husk leaf, whereas RHW1 overexpression yielded a wider husk leaf. RHW1 positively regulated the expression of ZCN4, a well-known TFL1-like protein involved in maize ear development. Dysfunction of ZCN4 reduced husk leaf width even in the context of RHW1 overexpression. The InDel variant in RHW1 is subject to selection and is associated with maize husk leaf adaption from tropical to temperate regions. Overall, our results identify that RHW1-ZCN4 regulates a pathway conferring husk leaf width variation at a very early stage of husk leaf development in maize. Overall design: RNA-seq liabraries were prepared using early developing ears (length, 0–0.5 cm) of rhw1-1, OE#1, and wild-type plants
Sample: RHW1-crispr-rep2
SAMN31712458 • SRS15744588 • All experiments • All runs
Organism: Zea mays
Library:
Name: GSM6730007
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA was extracted using RNAprep Pure Plant Plus kit,treated with RNase-free DNaseI and purified using the RNAclean Kit. RNA libraries for RNA-seq were prepared using NEBNext Ultra II RNA Library Prep kit following manufacturer's protocols.
Runs: 1 run, 26.9M spots, 8.1G bases, 2.4Gb
Run# of Spots# of BasesSizePublished
SRR2227380026,921,2078.1G2.4Gb2023-12-25

ID:
25234523

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