Tubulin synthesis during ciliogenesis in the mouse oviduct
We reported earlier that tubulin levels increase in the developing mouse oviduct during that period after birth when ciliogenesis is at a maximum (Staprans, I., and Dirksen, E. R. (1974) J. Cell Biol., 62, 164). To determine the degree to which de novo synthesis and tubulin pools contribute to this...
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Veröffentlicht in: | Developmental biology 1975-09, Vol.46 (1), p.1-13 |
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Sprache: | eng |
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Zusammenfassung: | We reported earlier that tubulin levels increase in the developing mouse oviduct during that period after birth when ciliogenesis is at a maximum (Staprans, I., and Dirksen, E. R. (1974)
J. Cell Biol.,
62, 164). To determine the degree to which
de novo synthesis and tubulin pools contribute to this increase, [
3H]leucine-incorporation experiments were performed
in vivo and in culture. Soluble, particulate and axonemal fractions, obtained from homogenized oviducts of 3-, 5-, 8- and 12-day-old suckling mice, were electrophoresed on sodium dodecyl sulfate gels and the specific activity of the tubulin band determined. The present work shows that more than 90% of the tubulin in 3-day-old and 75% in 5-day-old mouse oviducts is synthesized
de novo. From both the
in vivo and in culture experiments we conclude that although tubulin pools are present in mouse oviduct, they are continuously being replenished by newly synthesized protein as there is a rapid outflow from the soluble and particulate to the axonemal fraction into structures such as basal bodies and cilia. This burst of
de novo tubulin synthesis corresponds to evidence from electron microscopic autoradiography, where label is present to a greater extent over centriole precursors and basal bodies than over other cell organelles. [
3H]leucine incorporation into tubulin was inhibited by cycloheximide, demonstrating that we are dealing with synthesis, while colchicine below 10
−3,
M concentration had no effect on tubulin assembly into axonemes. |
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ISSN: | 0012-1606 1095-564X |
DOI: | 10.1016/0012-1606(75)90082-2 |