2016
DOI: 10.1016/j.fsi.2016.04.139
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Characterization of three mitogen-activated protein kinases (MAPK) genes reveals involvement of ERK and JNK, not p38 in defense against bacterial infection in Yesso scallop Patinopecten yessoensis

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Cited by 35 publications
(22 citation statements)
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“…Our results showed that ChERK mRNA was widely distributed in all of the tested developmental stages, with high expression at the trocophore stage (Fig. 4B), which is largely similar to Patinopecten yessoensis ERK [45] and other MAPK members in oyster [40,41]. These expression profiles suggested that ChERK might be similar to homologous genes in other species play a regulatory role in the embryonic development processes of the Hong Kong oyster.…”
Section: Cherk Was Broadly Expressed In Various Tissues and Differentsupporting
confidence: 52%
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“…Our results showed that ChERK mRNA was widely distributed in all of the tested developmental stages, with high expression at the trocophore stage (Fig. 4B), which is largely similar to Patinopecten yessoensis ERK [45] and other MAPK members in oyster [40,41]. These expression profiles suggested that ChERK might be similar to homologous genes in other species play a regulatory role in the embryonic development processes of the Hong Kong oyster.…”
Section: Cherk Was Broadly Expressed In Various Tissues and Differentsupporting
confidence: 52%
“…3, ChERK was localized to the mollusk cluster with previously reported ERK sequences from Tegillarca granosa, Crassostrea gigas and Aplysia californica. Multiple sequence alignment and phylogenetic analysis showed that ChERK shared high homology with other reported ERKs, especially with those of mollusk species [44,45], which further demonstrated that ChERK belongs to the ERK family. Previous studies showed that the classic mammalian ERK family includes two highly homologous isoforms (ERK1 and ERK2), whereas only one classic ERK homologue is reported in some lower invertebrate species, including Drosophila melanogaster, Litopenaeus vannamei and Patinopecten yessoensis [34,45e48].…”
Section: Cloning and Characterization Of Cherk Sequencementioning
confidence: 68%
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“…TGF-β1, a fibrotic stimulus, is able to activate Smad proteins (Smad2 or Smad3) directly to cause renal fibrosis (31)(32)(33)(34). Mitogen-activated protein kinase (MAPK) pathways, which comprise extracellular signal-regulated kinase (ERK), c-JUN N-terminal kinase (JNK) and p38 signaling, have been reported to play a role in inflammatory regulation (35,36), and also contribute to the amplification of transmitted signals to promote cellular processes, including proliferation and differentiation, either in the cytoplasm or nucleus (37,38). Thus, the current study aimed to investigate two areas: Firstly, whether there is a cross-talk effect between Smad3 and MAPKs in glomerulosclerosis; and secondly, whether the phosphorylation of MAPKs may be mediated by EP4 receptors.…”
Section: Introductionmentioning
confidence: 99%