Characterization of phi112, a Molecular Marker Tightly Linked to the o2 Gene of Maize, and Its Utilization in Multiplex PCR for Differentiating Normal Maize from QPM.
Alla SinghChikkappa KarjagiSehgeet KaurGagan JeetDeepak BhamareSonu GuptaSunil KumarAbhijit DasMamta GuptaDharam Paul ChaudharyBharat BhushanB S JatRamesh KumarM C DaglaManoj KumarPublished in: Genes (2023)
Quality Protein Maize (QPM) contains higher amounts of essential amino acids lysine and tryptophan. The QPM phenotype is based on regulating zein protein synthesis by opaque2 transcription factor. Many gene modifiers act to optimize the amino acid content and agronomic performance. An SSR marker, phi112, is present upstream of the opaque2 DNA gene. Its analysis has shown the presence of transcription factor activity. The functional associations of opaque2 have been determined. The putative transcription factor binding at phi112 marked DNA was identified through computational analysis. The present study is a step towards understanding the intricate network of molecular interactions that fine-tune the QPM genotype to influence maize protein quality. In addition, a multiplex PCR assay for differentiation of QPM from normal maize is shown, which can be used for Quality Control at various stages of the QPM value chain.
Keyphrases
- amino acid
- transcription factor
- genome wide identification
- dna binding
- quality control
- genome wide
- copy number
- single molecule
- real time pcr
- high throughput
- circulating tumor
- protein protein
- binding protein
- small molecule
- cell free
- magnetic resonance imaging
- air pollution
- dna methylation
- computed tomography
- magnetic resonance
- contrast enhanced
- genome wide analysis