Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
1999-6-9
pubmed:abstractText
Single-channel recordings of the currents mediated by the muscle Cl- channel, ClC-1, expressed in Xenopus oocytes, provide the first direct evidence that this channel has two equidistant open conductance levels like the Torpedo ClC-0 prototype. As for the case of ClC-0, the probabilities and dwell times of the closed and conducting states are consistent with the presence of two independently gated pathways with approximately 1.2 pS conductance enabled in parallel via a common gate. However, the voltage dependence of the common gate is different and the kinetics are much faster than for ClC-0. Estimates of single-channel parameters from the analysis of macroscopic current fluctuations agree with those from single-channel recordings. Fluctuation analysis was used to characterize changes in the apparent double-gate behavior of the ClC-1 mutations I290M and I556N causing, respectively, a dominant and a recessive form of myotonia. We find that both mutations reduce about equally the open probability of single protopores and that mutation I290M yields a stronger reduction of the common gate open probability than mutation I556N. Our results suggest that the mammalian ClC-homologues have the same structure and mechanism proposed for the Torpedo channel ClC-0. Differential effects on the two gates that appear to modulate the activation of ClC-1 channels may be important determinants for the different patterns of inheritance of dominant and recessive ClC-1 mutations.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-1379744, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-1659664, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-1659665, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-2174129, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-2455224, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-6130538, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-6270629, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-7522344, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-7646898, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-7845466, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-7938226, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-7981750, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-8112288, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-8130334, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-8559248, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-8842208, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-8845168, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-8848046, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-8848047, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-8894974, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-8961185, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-8997669, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-9046241, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-9158157, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-9251795, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-9326936, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-9370423, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-9558482, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-9565403, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-9566422, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-9716133, http://linkedlifedata.com/resource/pubmed/commentcorrection/10051520-9736777
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0022-1295
pubmed:author
pubmed:issnType
Print
pubmed:volume
113
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
457-68
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1999
pubmed:articleTitle
The muscle chloride channel ClC-1 has a double-barreled appearance that is differentially affected in dominant and recessive myotonia.
pubmed:affiliation
Istituto di Cibernetica e Biofisica, CNR, I-16149 Genova, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't