bioRxiv Science⌕ Search

Biology subjects

Soni, K. K.

Publications and source records attributed to Soni, K. K..

2 recordsLinked to original sources

Tapetum specific TA29 promoter is regulated by cis- elements binding to positive and negative regulators

The TA29 gene from Nicotiana tabacum was one of the first tapetum-specific genes identified in 1990. Its promoter has been successfully used to develop barnase/barstar gene-based male sterility and restorer transgenic lines for hybrid seed production in crops such as mustard. Despite its biotechnological significance, no major studies have been conducted to delineate the regulatory mechanisms of its promoter. The presented work identifies critical cis-elements of the promoter, starting with in-silico analysis followed by functional validation through mutational studies and promoter activity analysis in transgenic tobacco lines. This work led to the identification of cis-elements that are putative binding sites for the transcription factors NtMYB12, NtGT-1a, NtNAG1, and NtLZ-HD. The binding sites for NtMYB12, NtGT-1a, and NtNAG1 act as positive regulators, whereas the binding site for NtLZ-HD functions as a negative regulator.

molecular biology↗

Engineering the AEG1 promoter from cotton to develop male sterile lines

This work reports on modifying the Upstream Regulatory Module (URM, 1.5 Kb region upstream of the open reading frame) of Anther Expressing Gene 1 (AEG1) from cotton to achieve anther specific activity. AEG1 was identified in a previous study aimed to isolate a promoter with tapetum specific activity. Such a promoter could then be used to express barnase and barstar genes for developing male sterile and restorer lines for hybrid seed production in cotton. The AEG1 URM was observed to be active in tapetum as well as in roots making it unusable to drive the expression of barnase gene. Analysis of the URM showed the presence of several root specific motifs. Two modified AEG1 URMs were developed, by removing or mutating these motifs and its activity checked in tobacco. The activity of one of the modified URMs, AEG1({Delta}Bmut) was restricted to the anther tissue as observed using the reporter gene {beta}-glucuronidase. The study also demonstrates that male sterile lines could be developed in tobacco using the AEG1({Delta}Bmut) URM to express the barnase gene. This work thus shows the possibility of engineering promoters to achieve tissue specificity and to develop male sterile lines in cotton.

plant biology↗