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1.
Genet Mol Res ; 15(4)2016 Nov 21.
Article in English | MEDLINE | ID: mdl-27886349

ABSTRACT

Sillago sihama (Forsskål, 1775), a commercially important marine fishery species in the Indo-West Pacific, is being developed as a target species for aquaculture and stock enhancement in China. However, due to the limitations of traditional isolation methods, the available microsatellite loci, or simple sequence repeats (SSRs), of S. sihama lack diversity. We used a stepwise approach including Illumina sequencing, primer screening, and SSR marker validation to develop diverse SSRs for S. sihama. A total of 853.48 Mb clean sequences were assembled with high coverage and sequencing depth, and 27,288 potential SSRs were identified. A set of 18 novel SSR markers with four type motifs including 11 di-, 1 tri-, 5 tetra-, and 1 hexanucleotide repeats were successfully isolated. The ranges of number of alleles per locus and observed and expected heterozygosities were 5-24, 0.226-0.968, and 0.319-0.950, respectively. The diversity parameters exhibited high levels of polymorphism in these 18 loci. Three loci with the presence of both null alleles and inbreeding showed significant deviation from Hardy-Weinberg equilibrium after Bonferroni correction. Moreover, 13 loci developed in S. sihama showed high transferability to the closely related species Sillago japonica. The polymorphic SSR markers developed in this study may serve as valuable tools for further basic and applied research on the genetic resources of S. sihama as well as S. japonica. Our results indicate that this approach, based on next-generation sequencing technology, is convenient, cost-effective, and suitable for SSR marker isolation in other sillaginid fishes.


Subject(s)
High-Throughput Nucleotide Sequencing/methods , Microsatellite Repeats , Perciformes/genetics , Sequence Analysis, DNA/methods , Animals , Aquaculture , China , Gene Frequency , Genetic Markers , Humans , Perciformes/growth & development
2.
Genet Mol Res ; 14(3): 7696-703, 2015 Jul 13.
Article in English | MEDLINE | ID: mdl-26214450

ABSTRACT

We aimed to investigate the influence of lentiviral-mediated Bcl-2 overexpression in cerebral tissues of rats with acute cerebral infarction. Forty-five rats were randomly divided into sham, model, and treatment groups. The sham and model groups were administered a control lentiviral vector via the intracranial arteries 10 days before surgery, while the treatment group received lentivirus encoding a Bcl-2 overexpression vector. We induced cerebral artery infarction using a suture-occlusion method and analyzed the cerebral expression levels of apoptosis-related genes (caspase-3, Bax), total cerebral apoptosis, range of cerebral tissue infarction, and changes in nerve cell function after 72 h. The Bcl-2-encoding lentivirus was well expressed in rat cerebral tissues. The treatment group had significantly higher expression levels of Bcl-2 than the other two groups. After cerebral infarction, the model group had significantly increased expression levels of caspase-3 and Bax protein in cerebral tissues than the sham (P < 0.05). Expression of these apoptosis-related proteins in the treatment group was obviously lower than that in the model group (P < 0.05), but significantly higher than in the sham group (P < 0.05). Compared to sham, neuronal apoptosis levels and infarction range of cerebral tissues was increased in the model and treatment groups; however, these values in the treatment group were significantly lower than that in the model group (P < 0.05). Importantly, the treatment group had significantly decreased neurological impairment scores (P < 0.05). In conclusion, Bcl-2 over-expression can decrease neuronal apoptosis in rat cerebral tissue, and thus is neuroprotective after cerebral ischemia.


Subject(s)
Cerebral Infarction/metabolism , Cerebral Infarction/pathology , Neurons/metabolism , Neuroprotective Agents/therapeutic use , Proto-Oncogene Proteins c-bcl-2/metabolism , Acute Disease , Animals , Apoptosis , Brain/metabolism , Brain/pathology , Caspase 3/metabolism , Cerebral Infarction/physiopathology , Neurons/pathology , Rats, Sprague-Dawley , bcl-2-Associated X Protein/metabolism
3.
Genet Mol Res ; 13(3): 4716-28, 2014 Jul 02.
Article in English | MEDLINE | ID: mdl-25062407

ABSTRACT

CBL-interacting protein kinases (CIPKs) mediate many plant responses to abiotic stress. However, their functions are poorly understood in halophytes. In this study, we isolated a CIPK gene, NtCIPK2, from the halophyte Nitraria tangutorum. By sequence alignment and the construction of a phylogenetic tree, we found that NtCIPK2 is similar to CIPK2 proteins from other plants, and contains conserved domains and motifs. The promoter of NtCIPK2 harbors many cis-acting elements that might be recognized and bound by transcription factors that are related to hormones and stress responses. NtCIPK2 was ubiquitously and robustly expressed in all tested organs, and was induced by salinity, drought, heat, and cold stress. The overexpression of NtCIPK2 in Escherichia coli caused better growth against high salinity, alkalinity, and osmotic conditions, dehydration, and extreme temperatures (i.e., heat and cold) compared to the control. Thus, NtCIPK2 is a candidate gene that might improve the stress tolerance of crops and herbs through genetic manipulation.


Subject(s)
Gene Expression Regulation, Plant , Magnoliaceae/genetics , Plant Proteins/genetics , Protein Serine-Threonine Kinases/genetics , Salt-Tolerant Plants/genetics , Amino Acid Sequence , Arabidopsis/enzymology , Arabidopsis/genetics , Cloning, Molecular , Cold Temperature , Droughts , Escherichia coli/genetics , Escherichia coli/metabolism , Hot Temperature , Magnoliaceae/classification , Magnoliaceae/enzymology , Molecular Sequence Data , Phylogeny , Plant Proteins/metabolism , Promoter Regions, Genetic , Protein Serine-Threonine Kinases/metabolism , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Salt Tolerance , Salt-Tolerant Plants/enzymology , Sequence Alignment , Stress, Physiological
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