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

Author:

Singh Alla1,Karjagi Chikkappa2ORCID,Kaur Sehgeet3,Jeet Gagan3,Bhamare Deepak1,Gupta Sonu1,Kumar Sunil1,Das Abhijit1,Gupta Mamta1,Chaudhary D. P.1ORCID,Bhushan Bharat1ORCID,Jat B. S.1,Kumar Ramesh1,Dagla M. C.1,Kumar Manoj4ORCID

Affiliation:

1. ICAR-Indian Institute of Maize Research, P.A.U. Campus, Ludhiana 141004, India

2. ICAR-Indian Institute of Maize Research, Pusa Campus, Delhi 110012, India

3. School of Agricultural Biotechnology, Punjab Agricultural University, Ludhiana 141004, India

4. ICAR—Central Institute for Research on Cotton Technology, Mumbai 400019, India

Abstract

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.

Funder

Department of Science and Technology

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

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