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1.
Blood Cells Mol Dis ; 43(2): 202-10, 2009.
Article in English | MEDLINE | ID: mdl-19442542

ABSTRACT

The serine protease thrombin is generated from its precursor, prothrombin, in the coagulation cascade and plays a central role in fibrin deposition and platelet activation mediated through the protease activated receptors. Knockdown of prothrombin in the zebrafish was previously shown to recapitulate the phenotype observed in prothrombin knockout mice, such as an absence of blood pericardial edema, and hemorrhage. However, the role of thrombin during embryogenesis is not fully understood. To find genes affected by potential thrombin signaling in embryogenesis before blood circulation, microarray analysis was performed using total RNA prepared from antisense-injected, knockdown embryos versus mismatch-injected at 20 h post fertilization. A total of 63 upregulated and downregulated genes were identified with duplicate microarrays using dye reversal and a two-fold difference limitation. Real time RT-PCR for 10 selected genes identified by the microarray confirmed the expression changes in these genes. One particular gene, phlda3, was at least eleven fold upregulated, and in situ hybridization revealed expansion of phlda3 expression in the central nervous system, branchial arches, and head endoderm in knockdown embryos. The identification of these genes regulated by thrombin according to microarray analysis should provide a greater understanding of the effects of thrombin activity in the early vertebrate embryo.


Subject(s)
Gene Expression Regulation, Developmental , Prothrombin/genetics , Thrombin/metabolism , Zebrafish/embryology , Zebrafish/genetics , Animals , Down-Regulation , Embryo, Nonmammalian/cytology , Embryo, Nonmammalian/drug effects , Embryo, Nonmammalian/metabolism , Gene Knockdown Techniques , Oligonucleotide Array Sequence Analysis , Oligonucleotides, Antisense/genetics , Thrombin/antagonists & inhibitors , Up-Regulation
2.
Virology ; 369(2): 234-44, 2007 Dec 20.
Article in English | MEDLINE | ID: mdl-17825342

ABSTRACT

The genome sequence of the Salmonella enterica serovar Anatum-specific, serotype-converting bacteriophage epsilon15 has been completed. The nonredundant genome contains 39,671 bp and 51 putative genes. It most closely resembles the genome of phiV10, an Escherichia coli O157:H7-specific temperate phage, with which it shares 36 related genes. More distant relatives include the Burkholderia cepacia-specific phage, BcepC6B (8 similar genes), the Bordetella bronchiseptica-specific phage, BPP-1 (8 similar genes) and the Photobacterium profundum prophage, P Pphipr1 (6 similar genes). epsilon15 gene identifications based on homologies with known gene families include the terminase small and large subunits, integrase, endolysin, two holins, two DNA methylase enzymes (one adenine-specific and one cytosine-specific) and a RecT-like enzyme. Genes identified experimentally include those coding for the serotype conversion proteins, the tail fiber, the major capsid protein and the major repressor. epsilon15's attP site and the Salmonella attB site with which it interacts during lysogenization have also been determined.


Subject(s)
Genome, Viral , Salmonella Phages/genetics , Salmonella enterica/virology , Amino Acid Sequence , Bacteriophage Typing , Base Sequence , DNA, Bacterial/genetics , DNA, Viral/genetics , Molecular Sequence Data , Salmonella Phages/classification , Salmonella Phages/physiology , Salmonella enterica/classification , Salmonella enterica/genetics , Sequence Homology, Nucleic Acid , Serotyping , Species Specificity , Viral Proteins/genetics , Virus Assembly , Virus Integration
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