Evidence map›Paper›PMID 32735815›Full record

ArticleCurrent biology : CB2020

The Tail of Kinesin-14a in Giardia Is a Dual Regulator of Motility.

Kuo-Fu Tseng, Keith J Mickolajczyk, Guangxi Feng, Qingzhou Feng, Ethiene S Kwok, Jesse Howe, Elisar J Barbar, Scott C Dawson, William O Hancock, Weihong Qiu

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 45% of its field
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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

10 authors at 3 institutions in 1 country.

Kuo-Fu TsengDepartment of Physics, Oregon State University, Corvallis, OR 97331, USA.
Keith J MickolajczykDepartment of Biomedical Engineering, Penn State University, University Park, PA 16802, USA; Intercollege Graduate Degree Program in Bioengineering, Penn State University, University Park, PA 16802, USA.
Guangxi FengDepartment of Physics, Oregon State University, Corvallis, OR 97331, USA.
Qingzhou FengDepartment of Biomedical Engineering, Penn State University, University Park, PA 16802, USA.
Ethiene S KwokDepartment of Physics, Oregon State University, Corvallis, OR 97331, USA.
Jesse HoweDepartment of Biochemistry and Biophysics, Oregon State University, Corvallis, OR 97331, USA.
Elisar J BarbarDepartment of Biochemistry and Biophysics, Oregon State University, Corvallis, OR 97331, USA.
Scott C DawsonDepartment of Microbiology, University of California, Davis, Davis, CA 95616, USA.
William O HancockDepartment of Biomedical Engineering, Penn State University, University Park, PA 16802, USA; Intercollege Graduate Degree Program in Bioengineering, Penn State University, University Park, PA 16802, USA.
Weihong QiuDepartment of Physics, Oregon State University, Corvallis, OR 97331, USA; Department of Biochemistry and Biophysics, Oregon State University, Corvallis, OR 97331, USA. Electronic address: weihong.qiu@physics.oregonstate.edu.
Oregon State University · USPennsylvania State University · USUniversity of California, Davis · US

Funding

Molecular mechanism of kinesin motilityR01GM076476 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI HANCOCK, WILLIAM OLAF · 2006 to 2019
$3.5M
Mechanistic Analysis of Kinesin-14 Motility and Regulation for Bipolar Spindle AssemblyR01GM127922 · NIGMS · OREGON STATE UNIVERSITY · PI QIU, WEIHONG · 2019 to 2023
$1.5M
A biophysical approach to elucidating the molecular mechanisms of mitotic inhibitor targetsF99CA223018 · NCI · PENNSYLVANIA STATE UNIVERSITY, THE · PI MICKOLAJCZYK, KEITH JOSEPH · 2017 to 2017
$33k
NCI NIH HHS F99 CA223018NIGMS NIH HHS R01 GM076476NIGMS NIH HHS R01 GM127922
6 · The paper itself

Abstract

Kinesin-14s are microtubule-based motor proteins that play important roles in mitotic spindle assembly [1]. Ncd-type kinesin-14s are a subset of kinesin-14 motors that exist as homodimers with an N-terminal microtubule-binding tail, a coiled-coil central stalk (central stalk), a neck, and two identical C-terminal motor domains. To date, no Ncd-type kinesin-14 has been found to naturally exhibit long-distance minus-end-directed processive motility on single microtubules as individual homodimers. Here, we show that GiKIN14a from Giardia intestinalis [2] is an unconventional Ncd-type kinesin-14 that uses its N-terminal microtubule-binding tail to achieve minus-end-directed processivity on single microtubules over micrometer distances as a homodimer. We further find that although truncation of the N-terminal tail greatly reduces GiKIN14a processivity, the resulting tailless construct GiKIN14a-Δtail is still a minimally processive motor and moves its center of mass via discrete 8-nm steps on the microtubule. In addition, full-length GiKIN14a has significantly higher stepping and ATP hydrolysis rates than does GiKIN14a-Δtail. Inserting a flexible polypeptide linker into the central stalk of full-length GiKIN14a nearly reduces its ATP hydrolysis rate to that of GiKIN14a-Δtail. Collectively, our results reveal that the N-terminal tail of GiKIN14a is a de facto dual regulator of motility and reinforce the notion of the central stalk as a key mechanical determinant of kinesin-14 motility [3].

Indexed as

Motor ActivityAdenosine TriphosphateGiardiaKinesinsMicrotubulesProtein MultimerizationAdenosine TriphosphateKinesinscentral stalkdark-field microscopykinesin-14microtubulesprocessivitysteppingTIRF microscopy

Identifiers

PMID32735815
PMCPMC7511442
OpenAlexW3045634045

What OpenQuestion holds

Textmetadata
LicenceTDM
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.