Plant and Cell Physiology Advance Access published online on January 28, 2009
Plant and Cell Physiology, doi:10.1093/pcp/pcp016
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The Chlamydomonas hatching enzyme, sporangin, is expressed in specific phases of the cell cycle and is localized to the flagella of daughter cells within sporangial cell wall
1 Division of Integrated Life science, Graduate School of Biostudies, Kyoto University, Kyoto, 606-8502 Japan
2 Department of Applied Science, Faculty of Science, Okayama University of Science, Okayama, 700-0005 Japan,
3 Department of Biology, Faculty of Science, Kobe University, Kobe, 657-8501 Japan
*Corresponding author: Dr. Takeaki Kubo. Email: kubot{at}lif.kyoto-u.ac.jp, Phone: +81-75-753-6390, Fax: +81-75-753-6127.
| Abstract |
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The timely breakdown of extracellular matrix (ECM) by proteolytic enzyme is essential for development, morphogenesis and cell proliferation in plant and animal cells. Sporangin of the unicellular green alga Chlamydomonas reinhardtii that mediates breakdown of the sporangial cell wall to liberate the daughter cells after cell division is characterized as a subtilase-like serine protease. The sporangin gene is specifically transcribed during S/M phase in a synchronized-vegetative cell cycle. In immuno-blot analyses using a polyclonal antibody raised against the sporangin polypeptide, the enzyme is synthesized after mitotic cell division and accumulated in the daughter cells before hatching. Immuno-fluorescence analyses showed that sporangin is localized to the flagella of the daughter cells within the sporangial cell wall, and released into the culture medium. The data suggest that sporangin is released from flagella concurrently with the digestion of sporangial cell wall, and then the daughter cells are hatched from the sporangia in the Chlamydomonas vegetative cell cycle.
Keywords: Cell cycle - Chlamydomonas reinhardtii - Flagella - Hatching enzyme - Subtilase-like serine protease
4 Present address: Department of Chemical and Biological Sciences, Faculty of Science, Japan Woman's University, Tokyo, 112-8681 Japan
(Received December 23, 2008; Accepted January 25, 2009)
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