Regulation of Prestalk‐specific Acid Phosphatase in Dictyostelium discoideum

Acid phosphatase–2, as characterized by gel electrophoresis under non‐denaturing conditions, is a convenient marker for prestalk cells in Dictyostelium discoideum. We have purified this prestalk‐specific enzyme and have examined its regulation during development. Under denaturing conditions, the enz...

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Published inDevelopment, growth & differentiation Vol. 28; no. 5; pp. 471 - 482
Main Authors TASAKA, MASAO, KAY, CAROLYN A., SOMMERVILLE, SHARON M., GRANT, AROLINE E., TSANG, ADRIAN S.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.09.1986
Japanese Society of Developmental Biologists
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Summary:Acid phosphatase–2, as characterized by gel electrophoresis under non‐denaturing conditions, is a convenient marker for prestalk cells in Dictyostelium discoideum. We have purified this prestalk‐specific enzyme and have examined its regulation during development. Under denaturing conditions, the enzyme has a molecular weight of 50,000 and an isoelectric point of 4.0. On the other hand, acid phosphatase‐I have a Mr‐55,000 polypeptide (AP1–55) and a minor Mr‐50,000 polypeptide (AP1–50) and both have diffuse isoelectric point from 3.4 to 4.1. Using monoclonal antibodies directed against acid phosphatase‐2 as probes, we showed that some acid phosphatase‐2 are newly synthesized at slug stage and some are converted from AP1–50 which was synthesized during ealy development.
Bibliography:Department of Haematology and Oncology, Hospital for Sick Children, Toronto, Ontario M5G 1X8.
National Institute for Basic Biology, Okazaki Japan.
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ISSN:0012-1592
1440-169X
DOI:10.1111/j.1440-169X.1986.00471.x