Sperm Morphogenesis in Wild - type and Fertilization - defective Mutants of Caenorhabditis elegans 26 SAMUEL WARD , YAIR ARGON

Taking advantage of conditions that allow spermatogenesis in vitro, the timing and sequence of morphological changes leading from the primary spermatocyte to the spermatozoon is described by light and electron microscopy . Together with previous studies, this allows a detailed description of the nuclear, cytoplasmic, and membrane changes occurring during spermatozoan morphogenesis . By comparison with wild type, abnormalities in spermatogenesis leading to aberrant infertile spermatozoa are found in six fertilization-defective ( fer) mutants . In fer-1 mutant males, spermatids appear normal, but during spermiogenesis membranous organelles (MO) fail to fuse with the sperm plasma membrane and a short, though motile, pseudopod is formed . In fer-2, fer-3, and fer-4 mutants, spermatids accumulate 48-nm tubules around their nuclei where the centriole and an RNA containing perinuclear halo would normally be . In all three mutants, spermatids still activate to spermatozoa with normal fusion of their MOs, but the pseudopods formed are aberrant in most fer-2 and fer-4 spermatozoa and in some fer-3 spermatozoa . In fer-5 mutant males, spermatozoa do not form . Instead, defective spermatids with crystalline inclusions and abnormal internal laminar membranes accumulate . In fer-6 mutant males, only a few spermatozoa form and these have defective pseudopods . These spermatozoa retain their fibrous bodies, a structure which normally disassembles in the spermatid . The time of appearance of developmental abnormalities in all of these mutants correlates with the temperature-sensitive periods for development of infertil-