Peptidyl-prolyl cis-trans isomerases (PPIases) are ubiquitous proteins which are essential for cis-trans isomerisation of peptide bonds preceding the proline residue. PPIases are categorized into four sub-families viz., cyclophilins, FK506-binding proteins (FKBPs), parvulins and protein phosphatase 2A phosphatase activators (PTPAs). Apart from catalysing the cis-trans isomerization, these proteins have also been implicated in diverse cellular functions. Though PPIases have been identified in several important crop plants, information on these proteins, except cyclophilins, is scanty in wheat. In order to understand the role of these genes in wheat, we carried out genome-wide identification using computational approaches. The present study resulted in identification of 71 FKBP (TaFKBP) 12 parvulin (TaPar) and 3 PTPA (TaPTPA) genes in hexaploid wheat genome, which are distributed on different chromosomes with uneven gene densities. The TaFKBP and TaPar proteins, besides PPIase domain, also contain additional domains, indicating functional diversification. In silico prediction also revealed that TaFKBPs are localized to ER, nucleus, chloroplast and cytoplasm, while the TaPars are confined to cytoplasm and nucleus. The TaPTPAs, on the contrary, appear to be present only in the cytoplasm. Evolutionary studies predicted that most of the TaFKBP, TaPar and TaPTPA genes in hexaploid wheat have been derived from their progenitor species, with some events of loss or gain. Syntenic analysis revealed the presence of many collinear blocks of TaFKBP genes in wheat and its sub-genome donors. qRT-PCR analysis demonstrated that expression of TaFKBP and TaPar genes is regulated differentially by heat stress, suggesting their likely involvement in thermotolerance. The findings of this study will provide basis for further functional characterization of these genes and their likely applications in crop improvement.

Plant scientists across the globe are interested in studying the root growth architecture of plants to understand different processes determining growth and development in plants. In the majority of cases, root growth-related experiments are carried out on petri plates filled with solid nutrient media. However, plants growing in these plates are often exposed to conditions that are not close to the natural conditions. Also, it is difficult to pour two different media on the same plate which is quite a useful feature to study the effect of specific treatment on plant growth. In the present work, we describe an improved and easy-to-use petri plate system useful for studying root growth characteristics of young plants grown over solid nutrient media. In comparison to the conventional methods, the present plate system offers an advantage in terms of facilitating the pouring of two different media in the same plate, avoiding contact of the aerial part of the plant with nutrient media, and ensuring the growth of roots under dark conditions. Briefly, two sections with horizontal apertures are provided across the length of the plate. While the upper section ensures that the aerial part of plants does not come in contact with nutrient media, the lower section facilitates the growth of roots in a second media having different nutrient compositions. The upper section is kept black, and a self-adhesive black film is provided to cover the root-growing region of the plate ensuring the growth of roots under dark conditions. The described plate, therefore, provides a convenient system to study root growth under conditions close to natural conditions and hence minimizing experimental artifacts.