Differential expression of PKC isoforms in developing zebrafish
Protein kinase C isozymes are a biologically diverse group of enzymes known to be involved in a wide variety of cellular processes. They fall into three families (conventional, novel and atypical) depending upon their mode of activation. Several classes of zebrafish neurons have been shown to expres...
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Published in: | International journal of developmental neuroscience Vol. 25; no. 3; pp. 155 - 164 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
01-05-2007
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Subjects: | |
Online Access: | Get full text |
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Summary: | Protein kinase C isozymes are a biologically diverse group of enzymes known to be involved in a wide variety of cellular processes. They fall into three families (conventional, novel and atypical) depending upon their mode of activation. Several classes of zebrafish neurons have been shown to express PKCα during development, but the expression of other isoforms remains unknown. In this study we performed immunohistochemistry to determine if zebrafish express various isoforms of PKC. We used antibodies to test for the presence of enzymes that are thought to be preferentially expressed in the nervous system (PKCγ, βII, δ, ɛ, θ and ζ). Here, we show that PKCγ, ɛ, θ and ζ are expressed in the zebrafish CNS. Anti‐PKCγ labels Rohon‐Beard sensory neurons and Mauthner cells. PKCɛ and ζ staining is widespread in the CNS, and PKCθ and βII are expressed in skeletal muscle, especially at intersegmental boundaries. Immunoblot experiments confirm the specificity of the antibodies in zebrafish and indicate that the fish isoforms of PKCγ, βII, ɛ and ζ are similar to the mammalian isoforms. Interestingly, PKCθ appears to be similar to PKCθII, which, to date, has been found exclusively in mouse testis, but not in the mammalian CNS. Overall, our findings indicate that several different PKC isoforms are expressed in zebrafish, and that Rohon‐Beard, Mauthner cells and muscle fibers preferentially express some isoforms over others. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0736-5748 1873-474X |
DOI: | 10.1016/j.ijdevneu.2007.02.003 |