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The floral function of AtSK31 is therefore likely to be an example of neo-functionalization after the duplication event that produced paralogous Group III loci in Arabidopsis.
Our current understanding of floral filter mechanisms is limited as this particular aspect of floral function has received less attention than floral attractants.
The study of floral function and flowering-plant diversification remains a vibrant evolutionary field.
In addition to floral function, another CC-type gene, ROXY19 (GRX480), has been shown to be upregulated by salicylic acid (SA) in Arabidopsis.
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Among other floral functions, MC is involved in the development of sepals in the first whorl, whereas TAG1 specifies carpel identity of fourth whorl organ primordia.
Homologs of two Arabidopsis GSK3 genes with genetically confirmed roles in floral development, AtSK11 and AtSK12, exhibit floral preferential expression in several basal angiosperms, suggesting evolutionary conservation of their floral functions.
In the present study, the Kas FLM allele lacks floral repressor function compared with Col FLM, similar to the Nd null allele.
Based on expression patterns, none of the Gerbera SQUA-like genes are likely to control flower organ identity in the sense of the floral A function.
In addition to these, 25 other putative MADS box transcription factors without floral homeotic function that are members of the MIKC, Mα, Mβ, Mγ, Mδ subfamilies were also found to be expressed in the floral transcriptome.
Historical dogma indicates that flower color serves as an important long-range visual signal allowing pollinators to detect the flowers, while floral guides function as close-range signals that direct pollinators to a reward.
For example, a semi-dominant mutation in RPL27aC affected multiple aspects of plant shoot development, including leaf patterning, inflorescence and floral meristem function, as well as seed set [ 16].
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