Comparative analysis of transformed potato microtubers and its non-transformed counterpart using some biochemical analysis along with inter simple sequence repeat (ISSR) marker

The rapid progress of transgenic biotechnology has significantly promoted the development and production of genetically modified (GM) crops. The aim of this study was to compare some compositional analysis and genetic variation of transformed potato microtubers (Solanum tuberosum L. Desiree) line (which harbor potato virus Y coat protein gene) with its conventional line in order to understand the metabolic and genomic changes associated with the transformation process. The constituents measured were: amino acids profile, minerals content, reducing sugar, vitamin C, total phenolic, total flavonoid, β-carotene and antioxidant activity. Also, PCR based assay using inter simple sequence repeat (ISSR) was employed to characterize the genetic variation between both lines. The data demonstrated that, there were no significant differences between the transformed and nontransformed line in total amount of amino acids, some minerals, total phenolic, total flavonoid and β- carotene contents. Obtained results of the ISSR profile was efficiently discriminated in both selected lines at DNA level. Generally, it was concluded that the transformed microtubers line was confirmed to be similar to that of the non-transformed microtubers line.Key words: Amino acids, genetic modification, phenolic content, reducing sugar, Solanum tuberosum

Genetic analysis of some Egyptian rice genotypes using RAPD, SSR and AFLP

nformation of genetic similarities and diversity among superior Egyptian rice genotypes is necessary for future rice breeding programs and derivation of plant lines. Genetic variability and relationships among seven Egyptian rice genotypes namely Giza 178, Giza177, Giza 175, Giza171 Giza 172, Sakha 102, and Sakha 101 were established by using eight RAPD primers, six SSR primer pairs, eight AFLP primer combinations. The level of polymorphism as revealed by RAPD, SSR and AFLP was 72.2, 90, and 67.9%, respectively. The highest genetic relationship as revealed by combined RAPD, SSR, and AFLP was detected between Giza 175 and Giza177 (83.4%), while the lowest similarity was found between Giza 178 and Sakha 101 (61.5%). Dendrograms derived from different techniques include minor differences inclustering pattern but did not affect the main grouping of the different genotypes. Moreover RAPD, SSR and AFLP-based dendrograms clustered the two genotypes Giza171 and Giza 172 together and the two genotypes Giza 175 and Giza 177 in the same cluster. RAPD, SSR, and AFLP techniques characterized the seven rice varieties by a large number of unique markers, which revealed 17, 4, and 65 unique markers, respectively. It could be concluded that each type of the three molecular approaches of DNA analysis could identify the different rice genotypes, and some of the Egyptian rice genotypes under investigation have probably originated from closely related ancestors and possess high degree of genetic similarity

Faecal immunochemical testing (FIT) in patients with signs or symptoms of suspected colorectal cancer (CRC): a joint guideline from the Association of Coloproctology of Great Britain and Ireland (ACPGBI) and the British Society of Gastroenterology (BSG)

Faecal immunochemical testing (FIT) has a high sensitivity for the detection of colorectal cancer (CRC). In a symptomatic population FIT may identify those patients who require colorectal investigation with the highest priority. FIT offers considerable advantages over the use of symptoms alone, as an objective measure of risk with a vastly superior positive predictive value for CRC, while conversely identifying a truly low risk cohort of patients. The aim of this guideline was to provide a clear strategy for the use of FIT in the diagnostic pathway of people with signs or symptoms of a suspected diagnosis of CRC. The guideline was jointly developed by the Association of Coloproctology of Great Britain and Ireland/British Society of Gastroenterology, specifically by a 21-member multidisciplinary guideline development group (GDG). A systematic review of 13 535 publications was undertaken to develop 23 evidence and expert opinion-based recommendations for the triage of people with symptoms of a suspected CRC diagnosis in primary care. In order to achieve consensus among a broad group of key stakeholders, we completed an extended Delphi of the GDG, and also 61 other individuals across the UK and Ireland, including by members of the public, charities and primary and secondary care. Seventeen research recommendations were also prioritised to inform clinical management

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with a lifetime risk of one in 350 people and an unmet need for disease-modifying therapies. We conducted a cross-ancestry genome-wide association study (GWAS) including 29,612 patients with ALS and 122,656 controls, which identified 15 risk loci. When combined with 8,953 individuals with whole-genome sequencing (6,538 patients, 2,415 controls) and a large cortex-derived expression quantitative trait locus (eQTL) dataset (MetaBrain), analyses revealed locus-specific genetic architectures in which we prioritized genes either through rare variants, short tandem repeats or regulatory effects. ALS-associated risk loci were shared with multiple traits within the neurodegenerative spectrum but with distinct enrichment patterns across brain regions and cell types. Of the environmental and lifestyle risk factors obtained from the literature, Mendelian randomization analyses indicated a causal role for high cholesterol levels. The combination of all ALS-associated signals reveals a role for perturbations in vesicle-mediated transport and autophagy and provides evidence for cell-autonomous disease initiation in glutamatergic neurons