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Mind bomb-binding partner RanBP9 plays a contributory role in retinal development

  • Kyeong Won Yoo
    ,
  • Maivannan Thiruvarangan
    ,
  • Yun Mi Jeong
    ,
  • Mi Sun Lee
    ,
  • Sateesh Maddirevula
    ,
  • Myungchull Rhee
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

Ran-binding protein family member, RanBP9 has been reported in various basic cellular mechanisms and neuropathological conditions including schizophrenia. Previous studies have reported that RanBP9 is highly expressed in the mammalian brain and retina; however, the role of RanBP9 in retinal development is largely unknown. Here, we present the novel and regulatory roles of RanBP9 in retinal development of a vertebrate animal model, zebrafish. Zebrafish embryos exhibited abundant expression of ranbp9 in developing brain tissues as well as in the developing retina. Yeast two-hybrid screening demonstrated the interaction of RanBP9 with Mind bomb, a component of Notch signaling involved in both neurogenesis and neural disease autism. The interaction is further substantiated by co-localization studies in cultured cells. Knockdown of ranbp9 resulted in retinal dysplasia with defective proliferation of retinal cells, downregulation of neuronal differentiation marker huC, elevation of neural proliferation marker her4, and alteration of cell cycle marker p57kip2. Expression of the Müller glial cell marker glutamine synthase was also affected in knockdown morphants. Our results suggest that Mind bombbinding partner RanBP9 plays a role during retinal cell development of zebrafish embryogenesis.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 271-279 (9 pages)

Journal (Volume, Issue Number)

Molecules and Cells (Volume 40, Issue 4)

Publication milestones

  • Published - 04/01/2017

Publication status

Published - 04/01/2017

ISSN

1016-8478

Publication IDs

  • Scopus: 85018434461
  • PubMed: 28359144

Publication metrics

Metrics

Scopus
citations
Fractional count
1
Fractional count
0.11
Fractional count
8
Fractional count
0.89
Fractional count
1
Fractional count
1
SciVal
FWCI
0.15
SciVal
Author count
9
SciVal
citations
2
SciVal
Paper percentile
44

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Citation count
6
Captures
34

Funding Details

This work was supported by the National R&D Program for Cancer Control (1020090) and National Research Foundation of Korea (NRF) grants funded by the Korean government Ministry of Science, ICT and Future Planning (MSIP) (2014R1A2A1A11053562, 2015M3A9A8029261).
FundersFunding numbers
National R&D Program for Cancer Control
1020090
MSIP
2014R1A2A1A11053562, 2015M3A9A8029261
NRF
-