Evidence map›Paper›PMID 3546333›Full record

ArticleThe Journal of cell biology1987

Microtubule dynamics in vivo: a test of mechanisms of turnover.

P J Sammak, G J Gorbsky, G G Borisy

Abstract read
In one paragraph

Article in The Journal of cell biology, 1987. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

44 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Microtubule release from the centrosome.Proceedings of the National Academy of Sciences of the United States of America · 1997
    Article
  10. Article
  11. Article
  12. Intrinsic microtubule stability in interphase cells.The Journal of cell biology · 1994
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

P J Sammak
G J Gorbsky
G G Borisy

Funding

MECHANISM AND CONTROL OF MICROTUBULE ASSEMBLYR01GM025062 · NIGMS · UNIVERSITY OF WISCONSIN MADISON · PI BORISY, GARY G · 1985 to 2003
$1.9M
XENOPUS OOCYTE NUCLEAR ENVELOPE STRUCTUREP41RR000570 · NCRR · UNIVERSITY OF WISCONSIN MADISON · 1985 to 1998
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MECHANISM AND CONTROL OF MICROTUBULE ASSEMBLYR37GM025062 · NIGMS · UNIVERSITY OF WISCONSIN MADISON · PI BORISY, GARY G · 1989 to 1998
–
NCRR NIH HHS RR00570NIGMS NIH HHS GM25062
6 · The paper itself

Abstract

Clarification of the mechanism of microtubule dynamics requires an analysis of the microtubule pattern at two time points in the same cell with single fiber resolution. Single microtubule resolution was obtained by microinjection of haptenized tubulin (fluorescein-tubulin) and subsequent indirect immunofluorescence with an antifluorescein antibody. The two time points in a single cell were, first, the time of photobleaching fluorescein-tubulin, and second, the time of fixation. The pattern of fluorescence replacement in the bleached zone during this time interval revealed the relevant mechanisms. In fibroblasts, microtubule domains in the bleached zone are replaced microtubule by microtubule and not by mechanisms that affect all microtubules simultaneously. Of the models we consider, treadmilling and subunit exchange along the length do not account for this observation, but dynamic instability can since it suggests that growing and shrinking microtubules coexist. In addition, we show that the half-time for microtubule replacement is shortest at the leading edge. Dynamic instability accounts for this observation if in general microtubules do not catastrophically disassemble from the plus end, but instead have a significant probability of undergoing a transition to the growing phase before they depolymerize completely. This type of instability we call tempered rather than catastrophic because, through limited disassembly followed by regrowth, it will preferentially replace polymer domains at the ends of microtubules, thus accounting for the observation that the half-time of microtubule domain replacement is shorter with proximity to the leading edge.

Indexed as

Cell LineFluorescent Antibody TechniqueHumansMaleMicrotubulesSkinTemperatureTubulinTubulin

Identifiers

PMID3546333
PMCPMC2114545

What OpenQuestion holds

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LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.