• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Evolution of dimorphic immunoproteasome subunit gene

Research Project

Project/Area Number 15K18587
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Evolutionary biology
Research InstitutionFujita Health University

Principal Investigator

Tsukamoto Kentaro  藤田保健衛生大学, 総合医科学研究所, 助教 (00582818)

Project Period (FY) 2015-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2016: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2015: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
Keywordsプロテアソーム / プロテアーゼ / 二型性 / 種を超えた多型 / 遺伝子進化 / 対立遺伝子 / 免疫プロテアソーム / 獲得免疫
Outline of Final Research Achievements

PSMB8 is one of the proteasome beta subunits with protease activity responsible for generating MHC class I presenting-peptides. PSMB8 gene of cartilaginous and bony fish has two (A and F) lineages showing about 20% differences of amino acid residues. In bony fish, two lineages are presented as dimorphic alleles maintaining for about 400 million years among species. To clarify the biological factors maintaining the dimorphic alleles, cleavage specificities were compared between A and F alleles. Whereas immunoproteasome containing A lineage of PSMB8 increased chymotrypsin-like activity compared with constitutive proteasome, it having F lineage of PSMB8 decreased. this result implied that two lineages of PSMB8 supply the MHC class I presenting-pepties with various C-terminal residues.

Report

(3 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report

URL: 

Published: 2015-04-16   Modified: 2018-03-22  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi