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The flagella of the green alga Scherffelia dubia are covered by scales which consist of acidic polysaccharides and glycoproteins. Experimental deflagellation results in the
regeneration of flagella complete with scales. During flagellar regeneration, scales are newly synthesized in the Golgi apparatus,
exocytosed and deposited on the growing flagella. Flagellar regeneration is dependent upon protein synthesis and N-glycosylation,
as it is blocked by cycloheximide and partially inhibited by tunicamycin. Metabolic labeling with [35S]methionine/cysteine demonstrated that scale-associated proteins were not newly synthesized during flagellar regeneration,
suggesting that the proteins deposited on regenerating flagella were drawn from a pool. Quantitative immunoelectron microscopy
using a monospecific antibody directed against a scale-associated protein of 126 kDa (SAP126) revealed that the pool of SAP126
was primarily located at the plasma membrane, with minor labeling of the scale reticulum and trans-Golgi cisternae, both before deflagellation and during flagellar regeneration. Since SAP126 was sequestered during flagellar
regeneration into secretory vesicles together with newly synthesized scales, it is concluded that the persistent presence
of SAP126 in the trans-Golgi cisternae during scale biogenesis requires retrograde transport of the protein from the plasma membrane to the Golgi
apparatus.
Received: 3 July 1999 / Accepted: 21 August 1999 相似文献
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Phagotrophic protists are capable of congregating at point sources of food within a few minutes, from distances of up to several cm in the case of ciliates, or several mm in the case of microflagellates. This is exemplified by four ciliate species and a heterotrophic flagellate. Congregation is accomplished by the combined effect of more than one type of chemosensory motile behaviour including "kinetic responses", "temporal-gradient sensing", and "helical klinotaxis". The results are discussed in terms of microscale patchiness in nature. 相似文献
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