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Dive into the research topics where Rakesh Srivastava is active.

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Featured researches published by Rakesh Srivastava.


Plant Physiology | 2006

The TATA-Box Sequence in the Basal Promoter Contributes to Determining Light-Dependent Gene Expression in Plants

Kanti Kiran; Suraiya A. Ansari; Rakesh Srivastava; Niraj Lodhi; Chandra Prakash Chaturvedi; Samir V. Sawant; Rakesh Tuli

A prototype 13-bp TATA-box sequence, TCACTATATATAG, was mutated at each nucleotide position and examined for its function in the core promoter. Specific nucleotides in the first TATA, the second TATA, as well as the flanking sequences influenced promoter function in transient transformation of tobacco (Nicotiana tabacum var Petit Havana) leaves. The effect of a given mutation on reporter gene expression in light versus dark was variable and sometimes contrasting. Some mutations, like T7 or A8→C or G, completely inactivated the expression of the minimal promoter in light but not in dark. In general, the sequence requirement for dark expression was less stringent than that for light expression. The selective effect of TATA-box mutations on light versus dark expression was exerted on core promoter function in the chromatin-integrated state also. Even in the presence of an upstream light response activator element, TATA-box mutations influenced modulation of the promoter by light. An A at the eighth position was specifically involved in the red light response of the promoter. Selectivity in gene expression was associated with a high level of transcript initiation from a site that was not active in the dark. Nuclear proteins from dark- and light-grown seedlings showed that the sequence variation within the TATA-box governs the formation of alternative transcriptional complexes. The experiments give direct evidence for the role of a core TATA-box sequence in determining the level as well as selectivity of gene expression in plants.


IEEE Transactions on Reliability | 1983

On Shrinkage Estimation of the Exponential Scale Parameter

B.N. Pandey; Rakesh Srivastava

This paper proposes some shrunken estimators for the scale parameter of an exponential distribution and compares them with the minimum mean squared error (MSE) estimator. The shrunken estimators have smaller MSE than the minimum MSE estimator when the prior estimate is good.


Molecular Plant | 2014

Distinct Role of Core Promoter Architecture in Regulation of Light-Mediated Responses in Plant Genes

Rakesh Srivastava; Krishan Mohan Rai; Meenal Srivastava; V. Kumar; Bindu Pandey; Sudhir P. Singh; Sumit K. Bag; B. D. Singh; Rakesh Tuli; Samir V. Sawant

In the present study, we selected four distinct classes of light-regulated promoters. The light-regulated promoters can be distinctly grouped into either TATA-box-containing or TATA-less (initiator-containing) promoters. Further, using either native promoters or their swapped versions of core promoter elements, we established that TATA-box and Inr (Initiator) elements have distinct mechanisms which are involved in light-mediated regulation, and these elements are not swappable. We identified that mutations in either functional TATA-box or Inr elements lead to the formation of nucleosomal structure. The nucleotide diversity in either the TATA-box or Inr element in Arabidopsis ecotypes proposes that the nucleotide variation in core promoters can alter the gene expression. We show that motif overrepresentation in light-activated promoters encompasses different specific regulatory motifs present downstream of TSS (transcription start site), and this might serve as a key factor in regulating light promoters which are parallel with these elements. Finally, we conclude that the TATA-box or Inr element does not act in isolation, but our results clearly suggests the probable involvement of other distinct core promoter elements in concurrence with the TATA-box or Inr element to impart selectivity to light-mediated transcription.


Acta Physiologiae Plantarum | 2015

Male sterility systems in wheat and opportunities for hybrid wheat development

Sudhir P. Singh; Rakesh Srivastava; Jitendra Kumar

The common wheat (Triticum aestivum L.) is a poly(hexa)ploid, derived from an amphi-diploidization process involving the donor species—Triticum urartu, Aegilops speltoides, Triticum turgidum, and Aegilops tauschii. The genetic diversity of the autogamous wheat is narrow, which is a major reason for lesser rate of yield gain in wheat, in contrast to rice and maize. It is desirable to encourage hybrid breeding, i.e., combining different lines into genetically divergent heterotic pools. Thus, hybrid plants are a unique combination of desired alleles produced by crossing between genetically different parental lines. Hybrid seed production in a crop requires male-sterile female parents along with a reliable outcrossing system. The male-sterile female parent prevents pollen shedding and self-fertilization, maintaining the purity of hybrid seeds. An outcrossing system enhances hybrid seed production. This article emphasizes the biological relevance of crossbreeding and self-pollination in wheat, and reviews different male sterility systems which could be utilized for the development of hybrid wheat. Several biotechnological approaches and their practical utility in generating cross-compatible male-sterile female parent lines have been discussed.


PLOS ONE | 2015

Spt-Ada-Gcn5-Acetyltransferase (SAGA) Complex in Plants: Genome Wide Identification, Evolutionary Conservation and Functional Determination

Rakesh Srivastava; Krishan Mohan Rai; Bindu Pandey; Sudhir P. Singh; Samir V. Sawant

The recruitment of RNA polymerase II on a promoter is assisted by the assembly of basal transcriptional machinery in eukaryotes. The Spt-Ada-Gcn5-Acetyltransferase (SAGA) complex plays an important role in transcription regulation in eukaryotes. However, even in the advent of genome sequencing of various plants, SAGA complex has been poorly defined for their components and roles in plant development and physiological functions. Computational analysis of Arabidopsis thaliana and Oryza sativa genomes for SAGA complex resulted in the identification of 17 to 18 potential candidates for SAGA subunits. We have further classified the SAGA complex based on the conserved domains. Phylogenetic analysis revealed that the SAGA complex proteins are evolutionary conserved between plants, yeast and mammals. Functional annotation showed that they participate not only in chromatin remodeling and gene regulation, but also in different biological processes, which could be indirect and possibly mediated via the regulation of gene expression. The in silico expression analysis of the SAGA components in Arabidopsis and O. sativa clearly indicates that its components have a distinct expression profile at different developmental stages. The co-expression analysis of the SAGA components suggests that many of these subunits co-express at different developmental stages, during hormonal interaction and in response to stress conditions. Quantitative real-time PCR analysis of SAGA component genes further confirmed their expression in different plant tissues and stresses. The expression of representative salt, heat and light inducible genes were affected in mutant lines of SAGA subunits in Arabidopsis. Altogether, the present study reveals expedient evidences of involvement of the SAGA complex in plant gene regulation and stress responses.


Plant Physiology | 2009

A T9G Mutation in the Prototype TATA-Box TCACTATATATAG Determines Nucleosome Formation and Synergy with Upstream Activator Sequences in Plant Promoters

Amol Ranjan; Suraiya A. Ansari; Rakesh Srivastava; Shrikant Mantri; Mehar Hasan Asif; Samir V. Sawant; Rakesh Tuli

We had earlier reported that mutations to G and C at the seventh and eighth positions in the prototype TATA-box TCACTATATATAG inhibited light-dependent activation of transcription from the promoter. In this study, we characterized mutations at the ninth position of the prototype TATA-box. Substitution of T at the ninth position with G or C enhanced transcription from the promoter in transgenic tobacco (Nicotiana tabacum) plants. The effect of T9G/C mutations was not light dependent, although the 9G/C TATA-box showed synergy with the light-responsive element (lre). However, the 9G/C mutants in the presence of lre failed to respond to phytochromes, sugar, and calcium signaling, in contrast to the prototype TATA-box with lre. The 9G/C mutation shifted the point of initiation of transcription, and transcription activation was dependent upon the type of activating element present upstream. The synergy in activation was noticed with lre and legumin activators but not with rbcS, Pcec, and PR-1a activators. The 9G mutation resulted in a micrococcal nuclease-sensitive region over the TATA-box, suggesting a nucleosome-free region, in contrast to the prototype promoter, which had a distinct nucleosome on the TATA-box. Thus, the transcriptional augmentation with mutation at the ninth position might be because of the loss of a repressive nucleosomal structure on the TATA-box. In agreement with our findings, the promoters containing TATAGATA as identified by genome-wide analysis of Arabidopsis (Arabidopsis thaliana) are not tightly repressed.


PLOS ONE | 2014

Comparative transcriptional profiling of two wheat genotypes, with contrasting levels of minerals in grains, shows expression differences during grain filling.

Sudhir P. Singh; Raja Jeet; Jitendra Kumar; Vishnu Shukla; Rakesh Srivastava; Shrikant Mantri; Rakesh Tuli

Wheat is one of the most important cereal crops in the world. To identify the candidate genes for mineral accumulation, it is important to examine differential transcriptome between wheat genotypes, with contrasting levels of minerals in grains. A transcriptional comparison of developing grains was carried out between two wheat genotypes- Triticum aestivum Cv. WL711 (low grain mineral), and T. aestivum L. IITR26 (high grain mineral), using Affymetrix GeneChip Wheat Genome Array. The study identified a total of 580 probe sets as differentially expressed (with log2 fold change of ≥2 at p≤0.01) between the two genotypes, during grain filling. Transcripts with significant differences in induction or repression between the two genotypes included genes related to metal homeostasis, metal tolerance, lignin and flavonoid biosynthesis, amino acid and protein transport, vacuolar-sorting receptor, aquaporins, and stress responses. Meta-analysis revealed spatial and temporal signatures of a majority of the differentially regulated transcripts.


Microelectronics Reliability | 1988

Shrinkage testimators for the variance of a normal distribution at single and double stages

B.N. Pandey; H.J. Malik; Rakesh Srivastava

Abstract This paper proposes some shrunken testimators at single and double stages for the variance of normal distribution when an initial estimate of σ 2 is available in the form of point estimate σ 0 2 . The proposed testimators have been obtained by selecting different shrinkage factors useful in different situations. Expressions for bais, mean squared error, relative bias and relative efficiency have been derived. Comparisons of different proposed estimators have been made and it is shown that by taking the square of the shrinkage factor considered in Adke et al. (1987), the better estimator can be obtained when σ 0 2 is in the vicinity of true value.


Microelectronics Reliability | 1987

A shrinkage testimator for scale parameter of an exponential distribution

B.N. Pandey; Rakesh Srivastava

Abstract A shrinkage testimator, based on a test of hypothesis when an initial estimate of the scale parameter is available, has been proposed. The salient feature of the proposed testimator is that, being dependent on the test statistic, it removes arbitrariness in the choice of the shrinkage factor for a given level of significance. Expressions for bias, mean square error and relative efficiency with respect to the conventional estimator have been derived. Also, it has been shown that by taking the square of the shrinkage factor the relative efficiency of the testimator can be increased.


International Journal of Risk Assessment and Management | 2009

Decontamination of soil contaminated with petroleum grease

G.W. Rathod; K.S. Rao; K.K. Gupta; Rakesh Srivastava; R.P. Tiwari; Jitendra Kumar

Contamination modifies the engineering properties of soil, thereby restricting its further use either as a construction material or as a supporting medium. Due to the scarcity of land, it becomes imperative to reuse the land for infrastructure developmental activities. Out of numerous soil contaminants, automobile grease is one of the most prominent. Considering the cumulative impact of contamination by grease on soil properties, its remediation has become inevitable. An experimental programme was undertaken to reclaim the soils contaminated with grease in this study. The performance of surfactant to remove the petroleum grease from soil and its effect on restoring the geotechnical properties was quantitatively evaluated. Locally available soil (clay with medium plasticity) was contaminated with varying percentages of grease, i.e., 3%, 6% and 9% by dry weight of soil. Geotechnical properties of virgin (0% grease), contaminated and decontaminated soils were determined. Surfactant, namely liquid organic cleaner (LOC) was employed to decontaminate the soil.

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Rakesh Tuli

Biotechnology Institute

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Samir V. Sawant

Council of Scientific and Industrial Research

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B.N. Pandey

Banaras Hindu University

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Bindu Pandey

Council of Scientific and Industrial Research

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Krishan Mohan Rai

Council of Scientific and Industrial Research

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Suraiya A. Ansari

National Botanical Research Institute

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Raja Jeet

Biotechnology Institute

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