Spermatogenesis in Tenebrio molitor (Tenebrionidae, Coleoptera): A Fine Structure and Anti‐tubulin Immunofluorescence Study

Abstract

AbstractSpermatogonia and both generations of spermatocytes of Tenebrio molitor possess conventional bipolar spindles with only few aster MTs. Spindles in metaphase spermatogonia are surrounded by fenestrated two‐layered cisternae and do not contain intraspindle membranes. In metaphase spermatocytes, a spindle envelope is missing, but intraspindle membranes are abundant. Mitochondria form long threads lateral to the nucleus in prophase I of meiosis. The elongated mitochondria also align parallel to the spindle apparatus in prometaphase I. As a consequence, the spindles reside in a cage formed of mitochondria. This arrangement may guarantee proper bisection of the chondriome during division. Cells are tightly packed during spermatogonial divisions and in prophase I, but large intercellular spaces develop when the first meiotic spindle assembles. Then, cytoplasmic bridges which persist between the cells as a result of incomplete cytokinesis appear as slender tubes. Anti‐tubulin immunofluorescence using an antibody against acetylated α‐tubulin revealed intense acetylation throughout spermatogonial mitosis but a low degree of α‐tubulin acetylation in meiotic spindles prior to telophase. This may indicate a high microtubule turnover in meiosis.