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IFT25 Links the Signal-Dependent Movement of Hedgehog Components to Intraflagellar Transport

  • Brian T. Keady
    ,
  • Rajeev Samtani
    ,
  • Kimimasa Tobita
    ,
  • Maiko Tsuchya
    ,
  • Jovenal T. San Agustin
    ,
  • John A. Follit
*Corresponding author for this work
  • University of Massachusetts Medical School
    ,
  • University of Pittsburgh
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

The intraflagellar transport (IFT) system is required for building primary cilia, sensory organelles that cells use to respond to their environment. IFT particles are composed of about 20 proteins, and these proteins are highly conserved across ciliated species. IFT25, however, is absent from some ciliated organisms, suggesting that it may have a unique role distinct from ciliogenesis. Here, we generate an Ift25 null mouse and show that IFT25 is not required for ciliary assembly but is required for proper Hedgehog signaling, which in mammals occurs within cilia. Mutant mice die at birth with multiple phenotypes, indicative of Hedgehog signaling dysfunction. Cilia lacking IFT25 have defects in the signal-dependent transport of multiple Hedgehog components including Patched-1, Smoothened, and Gli2, and fail to activate the pathway upon stimulation. Thus, IFT function is not restricted to building cilia where signaling occurs, but also plays a separable role in signal transduction events.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 940-951 (12 pages)

Journal (Volume, Issue Number)

Developmental Cell (Volume 22, Issue 5)

Publication milestones

  • Published - 05/15/2012

Publication status

Published - 05/15/2012

ISSN

1534-5807

Publication IDs

  • Scopus: 84860898145
  • PubMed: 22595669

Publication metrics

Metrics

SciVal
citations
134
Scopus
citations
SciVal
FWCI
4.20
SciVal
Author count
10
SciVal
Paper percentile
98
SciVal
Top percentile
5
Fractional count
1
Fractional count
0.10
Fractional count
9
Fractional count
0.90
Fractional count
1
Fractional count
1

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Citation count
201
Captures
168

Funding Details

We thank Drs. S. Jones (Transgenic Mouse Core), G. Hendricks (Electron Microscopy Core), and P. Furcinitti (Digital Imaging Core) for assistance during this work and Dr. R. Bloodgood for carefully reading the manuscript. We also thank Dr. P. Odgren for use of his bright-field microscope, and Drs. J. Eggenschwiler (Princeton Univ) and R. Rohatgi (Stanford Univ) for reagents. This work was supported by the National Institutes of Health (GM060992 to G.J.P.) and (5U01HL098180 to C.W.L.). Core resources supported by the Diabetes Endocrinology Research Center grant DK32520 were also used.
FundersFunding numbers
Diabetes and Endocrinology Research Center
-
NIH
GM060992, 5U01HL098180
NIDDK
P30DK032520