Regulation of Membrane Fusion Events During Caenorhabditis elegans Spermatogenesis
Abstract (Summary)
FER-1 is required for fusion of specialized vesicles, called membranous
organelles, with the sperm plasma membrane during Caenorhabditis elegans
spermiogeneis. To investigate the role of FER-1 in membranous organelle
fusion, I first examined ten fer-1 mutations and found that they all cause the
same defect in membrane fusion. FER-1 and the ferlin protein family are
membrane proteins with four to seven C2 domains which commonly mediate
Ca2+-dependent lipid-processing events. Most of the fer-1 mutations fall within
these C2 domains, showing that they have distinct, non-redundant functions. I
found that membranous organelle fusion requires intracellular Ca2+ and that C2
domain mutations alter Ca2+ sensitivity. This suggests that the C2 domains are
involved in Ca2+ sensing and further supports their independent function. Using
two immunological approaches we found three FER-1 isoforms, two of which
may arise from FER-1 by proteolysis. By both light and electron microscopy
these FER-1 proteins are localized to membranous organelle membranes.
Together, these results suggest that the ferlin family members may share a
conserved mechanism to regulate cell-type specific membrane fusion.
In Chapter III, I present additional results toward studying the function of
FER-1 using several broad-based approaches. First, I present a bioinformatics
analysis of FER-1 C2 domains and the preliminary results of their calciumdependent
phospholipid binding capabilities. Second, preliminary interactions
found with individual FER-1 functional domains by a yeast-two hybrid screen are
discussed. Lastly, I present results from a candidate-gene approach to identify
additional regulators of MO fusion, the sperm-specific synaptobrevins.
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Bibliographical Information:
Advisor:
School:The University of Arizona
School Location:USA - Arizona
Source Type:Master's Thesis
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