TY - JOUR
T1 - The yeast Batten disease orthologue Btn1 controls endosome-Golgi retrograde transport via SNARE assembly
AU - Kama, Rachel
AU - Kanneganti, Vydehi
AU - Ungermann, Christian
AU - Gerst, Jeffrey
N1 - Israel Science Foundation [188/07, 358/10]; Y. Leon Benoziyo Institute for Molecular Medicine; Irving B. Harris Foundation; Weizmann Institute of Science; National Contest for Life Foundation; Deutsche Forschungsgemeinschaft [SFB 944, 431]; Hans-Muhlenhoff FoundationThis study was supported by grants to J.E. Gerst from the Israel Science Foundation (188/07 and 358/10), Y. Leon Benoziyo Institute for Molecular Medicine, Irving B. Harris Foundation, and Weizmann Institute of Science and to V. Kanneganti and J.E. Gerst from the National Contest for Life Foundation. C. Ungermann is supported by grants from the Deutsche Forschungsgemeinschaft (SFB 944 and 431) and Hans-Muhlenhoff Foundation. J.E. Gerst holds the Besen-Brender Chair of Microbiology and Parasitology.
PY - 2011/10/17
Y1 - 2011/10/17
N2 - The human Batten disease gene CLN3 and yeast orthologue BTN1 encode proteins of unclear function. We show that the loss of BTN1 phenocopies that of BTN2, which encodes a retromer accessory protein involved in the retrieval of specific cargo from late endosomes (LEs) to the Golgi. However, Btn1 localizes to Golgi and regulates soluble N-ethyl-maleimide sensitive fusion protein attachment protein receptor (SNARE) function to control retrograde transport. Specifically, BTN1 overexpression and deletion have opposing effects on phosphorylation of the Sed5 target membrane SNARE, on Golgi SNARE assembly, and on Golgi integrity. Although Btn1 does not interact physically with SNAREs, it regulates Sed5 phosphorylation by modulating Yck3, a palmitoylated endosomal kinase. This may involve modification of the Yck3 lipid anchor, as substitution with a transmembrane domain suppresses the deletion of BTN1 and restores trafficking. Correspondingly, deletion of YCK3 mimics that of BTN1 or BTN2 with respect to LE-Golgi retrieval. Thus, Btn1 controls retrograde sorting by regulating SNARE phosphorylation and assembly, a process that may be adversely affected in Batten Disease patients.
AB - The human Batten disease gene CLN3 and yeast orthologue BTN1 encode proteins of unclear function. We show that the loss of BTN1 phenocopies that of BTN2, which encodes a retromer accessory protein involved in the retrieval of specific cargo from late endosomes (LEs) to the Golgi. However, Btn1 localizes to Golgi and regulates soluble N-ethyl-maleimide sensitive fusion protein attachment protein receptor (SNARE) function to control retrograde transport. Specifically, BTN1 overexpression and deletion have opposing effects on phosphorylation of the Sed5 target membrane SNARE, on Golgi SNARE assembly, and on Golgi integrity. Although Btn1 does not interact physically with SNAREs, it regulates Sed5 phosphorylation by modulating Yck3, a palmitoylated endosomal kinase. This may involve modification of the Yck3 lipid anchor, as substitution with a transmembrane domain suppresses the deletion of BTN1 and restores trafficking. Correspondingly, deletion of YCK3 mimics that of BTN1 or BTN2 with respect to LE-Golgi retrieval. Thus, Btn1 controls retrograde sorting by regulating SNARE phosphorylation and assembly, a process that may be adversely affected in Batten Disease patients.
UR - http://www.scopus.com/inward/record.url?scp=80155138564&partnerID=8YFLogxK
U2 - https://doi.org/10.1083/jcb.201102115
DO - https://doi.org/10.1083/jcb.201102115
M3 - مقالة
SN - 0021-9525
VL - 195
SP - 203
EP - 215
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 2
ER -