Localised chiasmata due to partial pairing: A 3D reconstruction of synaptonemal complexes in male Stethophyma grossum

TLDR: The possible role of localised pairing as a mechanism producing localised chiasmata in Stethophyma grossum spermatocytes has been examined ultrastructurally and suggests that the shortest bivalent paired very quickly, the longer ones progressively slower, and that pairing proceeded zip-like from a point at or very close to the end attached to the nuclear envelope.

Abstract: The possible role of localised pairing as a mechanism producing localised chiasmata in Stethophyma grossum spermatocytes has been examined ultrastructurally. Nuclei at four successive stages of meiosis from leptotene to pachytene were reconstructed from a series of ultrathin sections and the extent of synapsis as demonstrated by synaptonemal complex (SC) formation was calculated. On the basis of the relative lengths of SCs and condensed chromosomes it was reasoned that only the centromeric ends of the long and medium length bivalents paired, and only one end of these SCs was found attached to the nuclear envelope. Only the three shortest bivalents paired completely, and both their SC ends were attached to the nuclear envelope. Thus pairing was directly related to the distribution of chiasmata. The extent of pairing at different stages suggests that the shortest bivalent paired very quickly, the longer ones progressively slower, and that pairing proceeded zip-like from a point at or very close to the end attached to the nuclear envelope, since all stretches of SC were attached to the envelope, and there were never more than 11 pieces, one for each bivalent. Chromosome decondensation and axial core formation did not occur far in advance of SC formation, and synapsis appeared to be much slower in S. grossum than in other species with non-localised chiasmata, as a larger proportion of the meiotic cysts were in “zygotene”, compared to Stauroderus scalaris and Locusta migratoria, although this was not quantified.