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Molecular Biology Reports

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https://www.readbyqxmd.com/read/29330722/location-of-low-copy-genes-in-chromosomes-of-brachiaria-spp
#1
Thaís Furtado Nani, James C Schnable, Jacob D Washburn, Patrice Albert, Welison Andrade Pereira, Fausto Souza Sobrinho, James A Birchler, Vânia Helena Techio
Repetitive DNA sequences have been widely used in cytogenetic analyses. The use of gene sequences with a low-copy-number, however, is little explored especially in plants. To date, the karyotype details in Brachiaria spp. are limited to the location of rDNA sites. The challenge lies in developing new probes based on incomplete sequencing data for the genus or complete sequencing of related species, since there are no model species with a sequenced genome in Brachiaria spp. The present study aimed at the physical location of conserved genes in chromosomes of Brachiaria ruziziensis, Brachiaria brizantha, and Brachiaria decumbens using RNAseq data, as well as sequences of Setaria italica and Sorghum bicolor through the fluorescent in situ hybridization technique...
January 12, 2018: Molecular Biology Reports
https://www.readbyqxmd.com/read/29330721/transcriptomic-analysis-and-discovery-of-genes-in-the-response-of-arachis-hypogaea-to-drought-stress
#2
Xiaobo Zhao, Chunjuan Li, Shubo Wan, Tingting Zhang, Caixia Yan, Shihua Shan
The peanut (Arachis hypogaea) is an important crop species that is threatened by drought stress. The genome sequences of peanut, which was officially released in 2016, may help explain the molecular mechanisms that underlie drought tolerance in this species. We report here a gene expression profiling of A. hypogaea to gain a global view of its drought resistance. Using whole-transcriptome sequencing, we analysed differential gene expression in response to drought stress in the drought-resistant peanut cultivar J11...
January 12, 2018: Molecular Biology Reports
https://www.readbyqxmd.com/read/29288425/polymorphisms-of-caprine-gnrhr-gene-and-their-association-with-litter-size-in-west-african-dwarf-goats
#3
M N Bemji, A M Isa, E M Ibeagha-Awemu, M Wheto
Gonadotropin-releasing hormone receptor (GnRHR) gene is considered a candidate gene for litter size due to its critical role in regulating the activities of hypothalamo-pituitary-gonadal axis which synthesizes and releases gonadotropins. This study was designed to identify mutations within the caprine GnRHR gene and investigate their association with litter size at various parities. Polymorphisms scanning and genotyping of GnRHR gene in West African Dwarf (WAD) goats (n = 226) revealed three single nucleotide polymorphisms (SNPs), one mutation (g...
December 29, 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/29288424/development-of-microsatellite-markers-for-myracrodruon-urundeuva-f-f-m-f-allem%C3%A3-o-a-highly-endangered-species-from-tropical-forest-based-on-next-generation-sequencing
#4
Danilla Cristina Lemos Souza, Bruno César Rossini, Francine Beatriz de Souza, Alexandre Magno Sebbenn, Celso Luís Marino, Mário Luiz Teixeira de Moraes
Myracrodruon urundeuva is a tree species of high economic importance due the strength and durability of its wood. Threatened of extinction in Brazil, it is present only in a few forest remnants, mostly in conservation units. Currently, there is little information on the genetic diversity of natural populations in Brazil and even less information about the genome of this species. Here, new species-specific microsatellite loci were developed based on next-generation sequencing (Illumina). More than 100,000 loci were identified in the run, with di- to hexanucleotides motifs...
December 29, 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/29282598/upf-proteins-highly-conserved-factors-involved-in-nonsense-mrna-mediated-decay
#5
REVIEW
Puneet Gupta, Yan-Ruide Li
Over 10% of genetic diseases are caused by mutations that introduce a premature termination codon in protein-coding mRNA. Nonsense-mediated mRNA decay (NMD) is an essential cellular pathway that degrades these mRNAs to prevent the accumulation of harmful partial protein products. NMD machinery is also increasingly appreciated to play a role in other essential cellular functions, including telomere homeostasis and the regulation of normal mRNA turnover, and is misregulated in numerous cancers. Hence, understanding and designing therapeutics targeting NMD is an important goal in biomedical science...
December 27, 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/29275442/development-of-microsatellite-markers-for-the-carnivorous-plant-genlisea-aurea-lentibulariaceae-using-genomics-data-of-ngs
#6
Yani C Aranguren-Díaz, Alessandro M Varani, Todd P Michael, Vitor F O Miranda
Genlisea aurea A.St.-Hil. is a carnivorous plant endemic species to Brazil in the Lentibulariaceae family. Very few studies have addressed the genetic structure and conservation status of G. aurea and the Lentibulariaceae. Microsatellites markers are advantageous tools that can be employed to predict the vulnerability of Lentibulariaceae species. Therefore, the development of molecular markers focusing the population analyses of Genlisea for future genetic studies and conservation actions are essential. Thus, we developed simple sequence repeats (SSRs) based on in silico analyses of G...
December 23, 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/29264734/genetics-and-genomics-of-susceptibility-and-immune-response-to-necrotic-enteritis-in-chicken-a-review
#7
REVIEW
Imran Zahoor, Abdul Ghayas, Atia Basheer
Global poultry production is facing many challenges and is currently under pressure due to the presence of several diseases like Necrotic Enteritis (NE). It is estimated that NE-caused global economic losses has increased from 2 billion to 6 billion US$ in 2015 because it is not easy to diagnose and control disease at the earlier stage of occurrence. Additionally, ban on the in-feed antibiotics and some other genetic and non-genetic predisposing factors affect the occurrence of the disease. Though the incidence of the disease can be reduced by minimizing the predisposing factors and through immunization of birds but there is no single remedy to control the disease...
December 20, 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/29264733/development-of-microsatellite-markers-using-next-generation-sequencing-for-the-fish-colossoma-macropomum
#8
Raquel B Ariede, Milena V Freitas, Milene E Hata, Vito A Matrochirico-Filho, Ricardo Utsunomia, Fernando F Mendonça, Fausto Foresti, Fábio Porto-Foresti, Diogo T Hashimoto
Tambaqui (Colossoma macropomum) is a fish species from the Amazon and Orinoco Rivers, with favorable characteristics to the cultivation system and great market acceptance in South America. However, the construction of a genetic map for the genetic improvement of this species is limited by the low number of molecular markers currently described. Thus, this study aimed to validate gene-associated and anonymous (non-genic) microsatellites obtained by next generation sequencing (RNA-seq and whole genome shotgun-WGS, respectively), for future construction of a genetic map and search for quantitative trait loci (QTL) in this species...
December 20, 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/29260368/development-of-13-microsatellite-markers-for-castanopsis-tribuloides-fagaceae-using-next-generation-sequencing
#9
Pimubon Waikham, Patcharawadee Thongkumkoon, Siriwadee Chomdej, Aizhong Liu, Prasit Wangpakapattanawong
Catanopsis tribuloides is a climax tree species commonly distributed in evergreen forests and has been used to restore degraded areas in northern Thailand. To aid in study of genetic diversity of the species, microsatellite markers, which are specific to C. tribuloides, were developed using whole genome sequencing by next-generation sequencing technology. The primers for microsatellite were developed and screened for optimal annealing temperature by PCR assay. The loci primers specific with C. tribuloides, 13 polymorphic microsatellite primers were successfully developed...
December 20, 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/29247288/characterization-of-genome-wide-microsatellite-markers-in-rabbitfishes-an-important-resource-for-artisanal-fisheries-in-the-indo-west-pacific
#10
Ilkser Erdem Kiper, Paulette Bloomer, Philippe Borsa, Thierry Bernard Hoareau
Rabbitfishes are reef-associated fishes that support local fisheries throughout the Indo-West Pacific region. Sound management of the resource requires the development of molecular tools for appropriate stock delimitation of the different species in the family. Microsatellite markers were developed for the cordonnier, Siganus sutor, and their potential for cross-amplification was investigated in 12 congeneric species. A library of 792 repeat-containing sequences was built. Nineteen sets of newly developed primers, and 14 universal finfish microsatellites were tested in S...
December 15, 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/29238890/real-time-detection-of-braf-v600e-mutation-from-archival-hairy-cell-leukemia-ffpe-tissue-by-nanopore-sequencing
#11
Davide Vacca, Valeria Cancila, Alessandro Gulino, Giosuè Lo Bosco, Beatrice Belmonte, Arianna Di Napoli, Ada Maria Florena, Claudio Tripodo, Walter Arancio
The MinION is a miniaturized high-throughput next generation sequencing platform of novel conception. The use of nucleic acids derived from formalin-fixed paraffin-embedded samples is highly desirable, but their adoption for molecular assays is hurdled by the high degree of fragmentation and by the chemical-induced mutations stemming from the fixation protocols. In order to investigate the suitability of MinION sequencing on formalin-fixed paraffin-embedded samples, the presence and frequency of BRAF c.1799T > A mutation was investigated in two archival tissue specimens of Hairy cell leukemia and Hairy cell leukemia Variant...
December 13, 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/29185131/nimbolide-attenuate-the-lipid-accumulation-oxidative-stress-and-antioxidant-in-primary-hepatocytes
#12
Ghedeir M Alshammari, Aristatile Balakrishnan, Thirunavukkarasu Chinnasamy
Nimbolide is a bioactive compound found in Azadirachta indica. This work was devised to investigate the potential effects of nimbolide on intracellular lipid deposition and its associated redox modulation in primary hepatocytes (Heps). Lipid accumulation was induced in Heps by supplementing 1 mM oleic acid for 24 h which was marked by significant accumulation of lipids. The results demonstrated that nimbolide can decrease intracellular cholesterol, free fatty acids and triglycerides. Nimbolide may also improve hepatocytes function through its antioxidant effects by inhibiting oxidative DNA damage and lipid peroxidation by curtailing the reactive oxygen species levels...
November 28, 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/29027636/polymorphisms-in-interleukins-17a-and-17f-genes-and-periodontitis-results-from-a-meta-analysis
#13
REVIEW
Felipe Rodolfo Pereira da Silva, Larissa Dos Santos Pessoa, Any Carolina Cardoso Guimarães Vasconcelos, Weberson de Aquino Lima, Even Herlany Pereira Alves, Daniel Fernando Pereira Vasconcelos
Polymorphisms in inflammatory genes such as interleukins 17A and 17F are associated with the risk of development of periodontitis, although the results remain contradictory. Hence, the aim of this study was perform a meta-analysis focusing on two polymorphisms (rs2275913 and rs763780) in interleukins 17A and 17F genes, respectively, in both chronic (CP) and aggressive periodontitis (AgP). A review in literature was performed in several databases for studies published before 25, September 2016. The meta-analysis was obtained through the review manager statistical software (version 5...
October 13, 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/29019065/correction-to-segregation-of-a-novel-p-ser270tyr-maf-mutation-and-p-tyr56-crygd-variant-in-a-family-with-dominantly-inherited-congenital-cataracts
#14
Lubica Dudakova, Viktor Stranecky, Olga Ulmanova, Eva Hlavova, Marie Trková, Andrea L Vincent, Petra Liskova
There was a spacing error in the initial online publication, and there were errors in the Acknowledgments section. The original article has been updated.
October 10, 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/28993955/the-c-29t-c-polymorphism-of-the-transforming-growth-factor-beta-1-tgfb1-gene-bone-mineral-density-and-the-occurrence-of-low-energy-fractures-in-patients-with-inflammatory-bowel-disease
#15
I Krela-Kaźmierczak, M Michalak, A Wawrzyniak, A Szymczak, P Eder, L Łykowska-Szuber, M Kaczmarek-Ryś, N Drwęska-Matelska, M Skrzypczak-Zielińska, K Linke, R Słomski
Gastrointestinal tract conditions are frequently associated with low bone mineral density and increased risk of fractures due to osteoporosis, the latter concerning particularly inflammatory bowel disease (IBD) patients. One of the candidate genes involved in osteoporosis is the transforming growth factor beta-1 (TGFB1) whose polymorphisms may be responsible for the development of this disease. The aim of this study was to analyse the frequency of TGFB1 polymorphic variants and determine the association between the c...
October 9, 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/28980161/sciatic-nerve-regeneration-by-transplantation-of-menstrual-blood-derived-stem-cells
#16
Saeed Farzamfar, Mahdi Naseri-Nosar, Alireza Ghanavatinejad, Ahmad Vaez, Amir Hassan Zarnani, Majid Salehi
This is the first study demonstrating the efficacy of menstrual blood-derived stem cell (MenSC) transplantation via a neural guidance conduit, for peripheral nerve regeneration. The synthesized poly (ɛ-caprolactone)/Gelatin conduit, filled with collagen type I and seeded with 3 × 10(4) MenSCs, was implanted into a rat's 10 mm sciatic nerve defect. The results of hot plate latency, sciatic functional index and weight-loss percentage of wet gastrocnemius muscle demonstrated that the MenSC transplantation had comparable nerve regeneration outcome to autograft, as the gold standard of nerve bridging...
October 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/28956216/creb-nf-y-and-meis1-conserved-binding-sites-are-essential-to-balance-myostatin-promoter-enhancer-activity-during-early-myogenesis
#17
Carla Vermeulen Carvalho Grade, Carolina Stefano Mantovani, Marina Alves Fontoura, Faisal Yusuf, Beate Brand-Saberi, Lúcia Elvira Alvares
Myostatin (MSTN) is a strong inhibitor of skeletal muscle growth in human and other vertebrates. Its transcription is controlled by a proximal promoter/enhancer (Mstn P/E) containing a TATA box besides CREB, NF-Y, MEIS1 and FXR transcription factor binding sites (TFBSs), which are conserved throughout evolution. The aim of this work was to investigate the role of these TFBSs on Mstn P/E activity and evaluate the potential of their putative ligands as Mstn trans regulators. Mstn P/E mutant constructs were used to establish the role of conserved TFBSs using dual-luciferase assays...
October 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/28951997/novel-compound-heterozygous-mutations-in-the-gpr98-ush2c-gene-identified-by-whole-exome-sequencing-in-a-moroccan-deaf-family
#18
Amale Bousfiha, Amina Bakhchane, Hicham Charoute, Mustapha Detsouli, Hassan Rouba, Majida Charif, Guy Lenaers, Abdelhamid Barakat
In the present work, we identified two novel compound heterozygote mutations in the GPR98 (G protein-coupled receptor 98) gene causing Usher syndrome. Whole-exome sequencing was performed to study the genetic causes of Usher syndrome in a Moroccan family with three affected siblings. We identify two novel compound heterozygote mutations (c.1054C > A, c.16544delT) in the GPR98 gene in the three affected siblings carrying post-linguale bilateral moderate hearing loss with normal vestibular functions and before installing visual disturbances...
October 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/28929467/erratum-to-hfe-mrna-expression-is-responsive-to-intracellular-and-extracellular-iron-loading-short-communication
#19
Kosha J Mehta, Sebastien Farnaud, Vinood B Patel
The original article has been changed to reflect the correct co-author name: Sebastien Farnaud. The original article was corrected.
October 2017: Molecular Biology Reports
https://www.readbyqxmd.com/read/28879539/synergistic-effect-of-two-%C3%AE-globin-gene-cluster-mutations-leading-to-the-hereditary-persistence-of-fetal-hemoglobin-hpfh-phenotype
#20
Priya Hariharan, Madhavi Sawant, Manju Gorivale, Ruma Manchanda, Roshan Colah, K Ghosh, Anita Nadkarni
Co-inheritance of gamma and beta globin gene mutations in a compound heterozygous state is rare but of clinical interest as it provides an important data on understanding the HbF expression. Hematological analysis was carried out (Sysmex KX-21). F-cells were enumerated using flow cytometry. Beta globin gene was analysed by CRDB technique and by DNA sequencing. Gamma globin promoter region was sequenced and expression studies were carried out using real time Taqman assay. We report a family, where two inherited defects of the β globin gene cluster segregate...
October 2017: Molecular Biology Reports
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