TL;DR: Six species of the genus Nephrotoma are added to the fauna of Xinjiang, and the following three species are recorded from China for the first time: N. analis, N. lundbecki l Lundbecki and N. tenuipes.
Abstract: Only four species of the genus Nephrotoma were previously known to occur in Xinjiang. Here six species are added to the fauna of Xinjiang. Among them Nephrotoma kanasensis sp. nov., is described and illustrated as new, and the following three species are recorded from China for the first time: N. analis (Schummel, 1833), N. lundbecki lundbecki (Nielsen, 1907) and N. tenuipes (Riedel, 1910). A key to the species of Nephrotoma from Xinjiang is presented.
TL;DR: Decorated actin-like filaments were seen in spindles after crane fly spermatocytes were glycerinated and then treated with rabbit skeletal muscle heavy meromyosin (HMM), suggesting that HMM in some way affects microtubule stability.
TL;DR: In this paper, the authors showed that actin-like filaments were seen near regions where chromosomal spindle fibres are seen in living cells, and were oriented in the pole-to-pole direction.
Abstract: Decorated actin-like filaments were seen in spindles after crane fly spermatocytes were glycerinated and then treated with rabbit skeletal muscle heavy meromyosin (HMM). Both ATP and pyrophosphate inhibited the HMM reaction. In prometaphase, metaphase, and mid-anaphase cells, actin-like filaments were seen near regions where chromosomal spindle fibres are seen in living cells, and were oriented in the pole-to-pole direction. In the interzone of anaphase cells, actin-like filaments were not oriented in a preferential direction when they were not associated with the microtubules attached to the sex chromosomes. No filaments were seen in glycerinated spindles not treated with HMM. We discuss reasons why filaments might not be seen without prior HMM treatment, and we discuss the possible role of the actin-like filaments in the spindles. — Spindle microtubules often were not seen in cells treated with HMM. This depended on the stage of division: in prometaphase no microtubules were seen; in metaphase microtubules were seen, in apparently normal numbers; in mid-anaphase, microtubules between the autosomes and the poles were seen in reduced numbers, those associated with the equatorial sex-chromosomes were seen in apparently normal numbers, while those between the separating autosomal half-bivalents were not seen. Microtubules were not seen in glycerinated spindles not treated with HMM, suggesting that HMM in some way affects microtubule stability. The question of microtubule stability is briefly discussed.
TL;DR: Actin-like filaments are seen at the cell periphery after crane fly spermatocytes are glycerinated and then treated with rabbit skeletal muscle heavy meromyosin this article.
Abstract: Actin-like filaments are seen at the cell periphery after crane fly spermatocytes are glycerinated and then treated with rabbit skeletal muscle heavy meromyosin. ATP and pyrophosphate inhibit the reaction with heavy meromyosin. From prometaphase through metaphase the filaments are all parallel to the cell surface, extending 0.5–1 μ. beneath the plasma membrane in a continuous layer of parallel filaments enveloping the cell; considering the poles of the spindle as north and south poles of the cell, the actin-like filaments at the cell periphery are all arranged as meridians. In late-anaphase, too, actin-like filaments are parallel to the cell surface, but here this includes bundles of filaments oriented as parallels in the furrow and adjacent regions of the cell periphery, as well as filaments oriented as meridians in the rest of the cell periphery. — Actin-like filaments are seen in the cellular projections associated with the spindle poles.
TL;DR: This observation supports the hypothesis that tubulin subunits add at the kinetochore in metaphase and that acetylation occurs subsequent to addition and may be useful as a marker in anaphase to distinguish between different hypotheses of chromosome motion.
Abstract: We studied the distribution of acetylated α-tubulin in the microtubules of spermatogenic cells from the crane fly Nephrotoma suturalis (Loew) using a mono-clonal antibody specific for acetylated α-tubulin (6-11B-1). We found that cells in all stages of spermatogenesis contained acetylated microtubules including primary spermatocytes, meiotic cells, spermatids, and sperm. A subset of the acety-lated microtubules (those in midbodies and flagella) were resistant to cold depolymerization. Newly polymerized microtubules in nondividing cells were not acetylated for up to 15 min. indicating that acetylation lagged behind polymerization. In spindles, newly polymerized microtubules were acetylated after 5 min. Antibodies to acetylated α-tubulin selectively stained chromosome-to-pole fibers in dividing cells, but the staining appeared to decrease and taper of at the kinetochores. This observation supports the hypothesis that tubulin subunits add at the kinetochore in metaphase and that acetylation occurs subsequent to addition. Further, this taper may be useful as a marker in anaphase, to distinguish between different hypotheses of chromosome motion.