Please use this identifier to cite or link to this item: https://une.intersearch.com.au/unejspui/handle/1959.11/4
Title: A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of CaV1.4 channel activation
Contributor(s): Hemara-Wahanui, A (author); Berjukow, S (author); Striessnig, J (author); Marksteiner, R (author); Hering, S (author); Maw, MA (author); Hope, CI (author); Dearden, PK (author); Wu, S  (author)orcid ; Wilson-Wheeler, J (author); Sharp, DM (author); Lundon-Treweek, P (author); Clover, GM (author); Hoda, JC (author)
Publication Date: 2005
DOI: 10.1073/pnas.0501907102
Handle Link: https://hdl.handle.net/1959.11/4
Abstract: Light stimuli produce graded hyperpolarizations of the photoreceptorplasma membrane and an associated decrease in a voltagegatedcalcium channel conductance that mediates release of glutamateneurotransmitter. The Cav1.4 channel is thought to be involved in this process. The CACNA1F gene encodes the poreforming subunit of the Cav1.4 channel and various mutations in CACNA1F cause X-linked incomplete congenital stationary night blindness (CSNB2). The molecular mechanism of the pathology underlying the CSNB2 phenotype remains to be established. Recent clinical investigations of a New Zealand family found a severe visual disorder that has some clinical similarities to, but is clearly distinct from, CSNB2. Here, we report investigations into the molecular mechanism of the pathology of this condition. Molecular genetic analyses identified a previously undescribed nucleotide substitution in CACNA1F that is predicted to encode an isoleucine to threonine substitution at CACNA1F residue 745. The I745T CACNA1F allele produced a remarkable approximately --30-mV shift in the voltage dependence of Cav1.4 channel activation and significantly slower inactivation kinetics in an expression system.These findings imply that substitution of this wild-type residue intransmembrane segment IIS6 may have decreased the energy required to open the channel. Collectively, these findings suggest that a gain-of-function mechanism involving increased Cav1.4 channel activity is likely to cause the unusual phenotype.
Publication Type: Journal Article
Source of Publication: PNAS: Proceedings of the National Academy of Sciences of the United States of America, 102(21), p. 7553-7558
Publisher: National Academy of Sciences
Place of Publication: United States
ISSN: 0027-8424
Field of Research (FOR): 060410 Neurogenetics
Peer Reviewed: Yes
HERDC Category Description: C1 Refereed Article in a Scholarly Journal
Statistics to Oct 2018: Visitors: 547
Views: 545
Downloads: 1
Appears in Collections:Journal Article

Files in This Item:
2 files
File Description SizeFormat 
Show full item record

SCOPUSTM   
Citations

90
checked on Nov 26, 2018

Page view(s)

92
checked on Dec 29, 2018
Google Media

Google ScholarTM

Check

Altmetric


Items in Research UNE are protected by copyright, with all rights reserved, unless otherwise indicated.