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Biology subjects

Kar, B.

Publications and source records attributed to Kar, B..

3 recordsLinked to original sources

Tissue specific de novo transcriptome sequencing and expression analysis of candidate genes for terpenoid biosynthesis in Piper longum.

Piper longum L. an economically important plant lacks adequate molecular resources towards unmasking molecular mechanisms for terpenoid biosynthesis. The transcriptome profiling generated 36.91 and 36.24 million raw reads in leaf and fruit tissue respectively. The de novo transcriptome assembly was performed with 36,688,460 and 36,011,305 clean reads, which subsequently produced 40,033 and 44,025 coding sequences (CDS) in leaf and fruit samples, respectively. The CDS were annotated using different databases such as Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG). These annotations resulted mining of various trait specific genes including important terpenoid biosynthesis genes. Presence of 53 and 58 terpenoid compounds in essential oils of leaf and fruit of long pepper have also been identified using GC-MS. Additionally, relative gene expression of eight terpenoid biosynthesis genes each for both leaf and fruit were conducted using real-time polymerase chain reaction (RT-PCR). For further genetic diversity study, 4085 and 4564 number of SSRs were identified in leaf and fruit, respectively. This study significantly contributes to the understanding of long pepper at the molecular level by expanding the available genetic resources. This paves the way to improve long pepper varieties and develop new genotype with desirable quality traits.

plant biology↗

A Singular Base Editing Platform for Polyfunctional Multiplex Engineering of Immune Cells

Current methods to engineer antigen-specific receptors rely on randomly integrating vectors or double-strand break induced targeted integration, both of which pose safety risks. To implement an all-in-one tool for multiplex knockout (KO) and knock in (KI), we expand the use of cytosine and adenine base editor (ABE) nickase activity to stimulate homology-directed repair (HDR) and insert clinically relevant chimeric antigen receptors (CARs) into specific loci. Through a novel sgRNA design strategy and a recombinant adeno-associated virus (rAAV) delivered DNA template, we enhanced the efficiency of ABE8e-stimulated HDR in human T cells. By combining KI of CD19-, CD33-, or mesothelin-targeting CARs with >95% quadplex gene KO (B2M/CD3{varepsilon}/PDCD1/CISH), we achieve single-step generation of highly functional off-the-shelf CAR T cell products with enhanced function. Importantly, we found no detectable translocations or significant off-target edits and demonstrated efficacy against multiple cancer lines, and a suppressive 3D spheroid culture model. This efficient engineering process of Iterative Nicking for Synchronous Engineered Reprogramming of T cells (INSERT) establishes a safe, simplified platform for advanced therapeutic CAR T engineering.

bioengineering↗

The FusX TALE Base Editor (FusXTBE) for rapid mitochondrial DNA programming of human cells in vitro and zebrafish disease models in vivo

Functional analyses of mitochondria have been hampered by few effective approaches to manipulate mtDNA and a lack of existing animal models. Recently a TALE-derived base editor was shown to induce C-to-T (or G-to-A) sequence changes in mtDNA. We report here the FusX TALE Base Editor (FusXTBE) to facilitate broad-based access to TALE mitochondrial base editing technology. TALE Writer is a de novo in silico design tool to map potential mtDNA base editing sites. FusXTBE was demonstrated to function with comparable activity to the initial base editor in human cells in vitro. Zebrafish embryos were used as a pioneering in vivo test system, with FusXTBE inducing 90+% editing efficiency in mtDNA loci, the first example of majority mtDNA heteroplasmy induction in any system. Gene editing specificity as precise as a single nucleotide was observed in vivo for a protein-coding gene. Non-destructive genotyping enables single animal mtDNA analyses for downstream biological functional genomics applications. FusXTBE is a new gene editing toolkit for exploring important questions in mitochondrial biology and genetics.

genetics↗