[PDF][PDF] Peroxisomes: a nexus for lipid metabolism and cellular signaling

IJ Lodhi, CF Semenkovich - Cell metabolism, 2014 - cell.com
Peroxisomes are often dismissed as the cellular hoi polloi, relegated to cleaning up reactive
oxygen chemical debris discarded by other organelles. However, their functions extend far …

A unified nomenclature for peroxisome biogenesis factors.

B Distel, R Erdmann, SJ Gould, G Blobel… - The Journal of cell …, 1996 - rupress.org
OR the past 10 years, there has been substantial progress in the field of peroxisome
biogenesis. One key to this progress has been the use of genetic approaches in a wide …

A molecular chaperone complex at the lysosomal membrane is required for protein translocation

FA Agarraberes, JF Dice - Journal of cell science, 2001 - journals.biologists.com
A group of cytosolic proteins are targeted to lysosomes for degradation in response to serum
withdrawal or prolonged starvation by a process termed chaperone-mediated autophagy. In …

Multiple PEX genes are required for proper subcellular distribution and stability of Pex5p, the PTS1 receptor: evidence that PTS1 protein import is mediated by a …

G Dodt, SJ Gould - The Journal of cell biology, 1996 - rupress.org
PEX5 encodes the type-1 peroxisomal targeting signal (PTS1) receptor, one of at least 15
peroxins required for peroxisome biogenesis. Pex5p has a bimodal distribution within the …

[HTML][HTML] Saccharomyces cerevisiae Pex3p and Pex19p are required for proper localization and stability of peroxisomal membrane proteins

EH Hettema, W Girzalsky, M van den Berg… - The EMBO …, 2000 - embopress.org
The mechanisms by which peroxisomal membrane proteins (PMPs) are targeted to and
inserted into membranes are unknown, as are the required components. We show that …

Peroxisome Degradation by Microautophagy in Pichia pastoris: Identification of Specific Steps and Morphological Intermediates

Y Sakai, A Koller, LK Rangell, GA Keller… - The Journal of cell …, 1998 - rupress.org
We used the dye N-(3-triethylammoniumpropyl)-4-(p-diethylaminophenylhexatrienyl)
pyridinium dibromide (FM4-64) and a fusion protein, consisting of the green fluorescent …

Peroxisome biogenesis

PE Purdue, PB Lazarow - Annual review of cell and …, 2001 - annualreviews.org
▪ Abstract Fifteen years ago, we had a model of peroxisome biogenesis that involved growth
and division of preexisting peroxisomes. Today, thanks to genetically tractable model …

Components involved in peroxisome import, biogenesis, proliferation, turnover, and movement

S Subramani - Physiological reviews, 1998 - journals.physiology.org
Subramani, Suresh. Components Involved in Peroxisome Import, Biogenesis, Proliferation,
Turnover, and Movement. Physiol. Rev. 78: 171–188, 1998.—In the decade that has …

Peroxisome synthesis in the absence of preexisting peroxisomes

ST South, SJ Gould - The Journal of cell biology, 1999 - rupress.org
Zellweger syndrome and related diseases are caused by defective import of peroxisomal
matrix proteins. In all previously reported Zellweger syndrome cell lines the defect could be …

Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane …

Y Matsuzono, N Kinoshita, S Tamura… - Proceedings of the …, 1999 - National Acad Sciences
At least 11 complementation groups (CGs) have been identified for the peroxisome
biogenesis disorders (PBDs) such as Zellweger syndrome, for which seven pathogenic …