The heterochronic maize mutant Corngrass1 results from overexpression of a tandem microRNA

By G. Chuck, A. Cigan, Koy Saeteurn, S. Hake. Nature Genetics, 2007

645 citations recorded by the source corpus.

Subfields: Molecular Biology, Plant Science

View Paper: https://www.semanticscholar.org/paper/9573f3023d89478399bd1f0688795bd7bd8ae561

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Citations in the corpus

miR156-regulated SPL transcription factors define an endogenous flowering pathway in Arabidopsis thaliana. (2009, neutral): “It will therefore be interesting to learn which contribution miR156 targets, which are also present in grasses (Chuck et al., 2007; Wang et al., 2005; Yang et al., 2008), make to flowering control in this group of plants.”
The control of developmental phase transitions in plants (2011, background): “Mutations in the miR172-binding site have been shown to result in the dominant allele of Ids1, tasselseed6 (Chuck et al., 2007b).”
Small RNAs and Their Roles in Plant Development (2009, background): “Intriguingly, the maize Cg1 mutant that overexpresses miR156 has reduced miR172 levels, which suggests that miR156 and miR172 may act in a linear pathway that coordinates vegetative and floral transitions (Chuck et al. 2007).”
Seasonal and developmental timing of flowering. (2010, background): “Studies of the juvenile to adult phase transition revealed that the role of a particular microRNA, miR156, is to promote the juvenile phase in Arabidopsis and maize, and one consequence of this promotion is to prevent precocious flowering (Wu and Poethig, 2006; Chuck et al., 2007).”
The sequential action of miR156 and miR172 regulates developmental timing in Arabidopsis. (2009, neutral): “Overexpression of miR156 in both Arabidopsis and maize prolongs the expression of juvenile vegetative traits and delays flowering ( Chuck et al., 2007a; Wu and Poethig, 2006), whereas overexpression of miR172 in Arabidopsis accelerates flowering (Aukerman and Sakai, 2003; Chen, 2004; Jung et al., 2”
Criteria for Annotation of Plant MicroRNAs (2008, background): “When two or more miRNA-producing stem-loops are arrayed in tandem on a single precursor, each stem loop is treated as a distinct locus (for instance, Zea mays MIR156b and MIR156c; Chuck et al., 2007).”