Abstract

Visinin-like protein-3, which is one of the neuronal calcium sensors, has been shown to be mainly expressed in cerebellar Purkinje cells, but cellular function of this protein has not yet been elucidated. We examined the tissue distribution of murine visinin-like protein-3 transcripts using real-time reverse transcription-PCR. Visinin-like protein-3 mRNA was found to be expressed in peripheral tissues. Particularly, the expression of the transcript in the thymus was significantly higher than in other peripheral tissues. In addition, B6RVTC1 thymoma cells robustly expressed visinin-like protein-3 mRNA. To identify a target protein of visinin-like protein-3, we performed a pull-down experiment using glutathione S-transferase-tagged visinin-like protein-3 and two-dimensional electrophoresis. We demonstrated that microsomal cytochrome b(5) was a Ca(2+)-dependent binding partner of visinin-like protein-3. In a co-immunoprecipitation experiment, it was observed that hippocalcin, as well as visinin-like protein-3, could interact with cytochrome b(5). Furthermore, we confirmed that the sequence Val(114)-Tyr(127) at the C-terminal tail of cytochrome b(5) is the minimal structural requirement for binding to visinin-like protein-3. In addition, the loop His(19)-His(25) at the N terminus of visinin-like protein-3 is essential for binding to cytochrome b(5). Microsomal cytochrome b(5) was also shown to be a potential activator of cytochrome P450. The present findings raise the possibility that visinin-like protein-3 may link Ca(2+) signaling to the machinery of microsomal monooxygenase complex composed of cytochrome b(5), cytochrome P450, and some reductases. This report provides the first evidence of an interaction between visinin-like protein-3 and microsomal cytochrome b(5).

Highlights

  • Calcium ions play an extremely important and essential role in inter- and intracellular signaling pathways

  • In the thymus, slightly higher expression of VILIP-3 was observed in comparison with that in other peripheral tissues

  • Using a GST pulldown experiment in conjunction with 2-DE and N-terminal amino acid sequencing, we confirmed that VILIP-3 was able to associate with microsomal cytochrome b5 in a calcium-dependent manner

Read more

Summary

Introduction

Calcium ions play an extremely important and essential role in inter- and intracellular signaling pathways. V3⌬N14-Y and V3⌬N25-Y (EYFP-tagged VILIP-3 truncated of N-terminal ϳ14 and ϳ25 residues) expression vectors were obtained by subcloning the PCR products into the HindIII/BamHI sites of pEYFP-N1. For the in vitro binding assay using GST-tagged cytochrome b5 mutants, 70 – 80% confluent 293T cells in one well of a 6-well plate were transfected by 2 ␮g of V3-F expression vector.

Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.