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1.
J Cell Biol ; 185(1): 129-45, 2009 Apr 06.
Article in English | MEDLINE | ID: mdl-19349583

ABSTRACT

Phosphatidic acid (PA) is postulated to have both structural and signaling functions during membrane dynamics in animal cells. In this study, we show that before a critical time period during rhabdomere biogenesis in Drosophila melanogaster photoreceptors, elevated levels of PA disrupt membrane transport to the apical domain. Lipidomic analysis shows that this effect is associated with an increase in the abundance of a single, relatively minor molecular species of PA. These transport defects are dependent on the activation state of Arf1. Transport defects via PA generated by phospholipase D require the activity of type I phosphatidylinositol (PI) 4 phosphate 5 kinase, are phenocopied by knockdown of PI 4 kinase, and are associated with normal endoplasmic reticulum to Golgi transport. We propose that PA levels are critical for apical membrane transport events required for rhabdomere biogenesis.


Subject(s)
Drosophila melanogaster/ultrastructure , Phosphatidic Acids/metabolism , Photoreceptor Cells/ultrastructure , 1-Phosphatidylinositol 4-Kinase/antagonists & inhibitors , 1-Phosphatidylinositol 4-Kinase/physiology , ADP-Ribosylation Factor 1/physiology , ADP-Ribosylation Factor 6 , ADP-Ribosylation Factors/physiology , Adaptor Protein Complex alpha Subunits/antagonists & inhibitors , Adaptor Protein Complex alpha Subunits/physiology , Animals , Cell Membrane/metabolism , Cell Membrane/ultrastructure , Diacylglycerol Cholinephosphotransferase/genetics , Drosophila Proteins/genetics , Drosophila Proteins/metabolism , Drosophila Proteins/physiology , Drosophila melanogaster/genetics , Drosophila melanogaster/growth & development , Dynamins/genetics , Dynamins/metabolism , Dynamins/physiology , Membrane Lipids/metabolism , Microscopy, Electron, Transmission , Phenotype , Phosphatidate Phosphatase/genetics , Phosphatidate Phosphatase/metabolism , Phospholipase D/metabolism , Phosphotransferases (Alcohol Group Acceptor)/genetics , Phosphotransferases (Alcohol Group Acceptor)/metabolism , Phosphotransferases (Alcohol Group Acceptor)/physiology , Photoreceptor Cells/metabolism , Photoreceptor Cells/physiology , RNA Interference
2.
Plant Cell ; 15(8): 1859-71, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12897258

ABSTRACT

The import of nucleus-encoded proteins into chloroplasts is mediated by translocon complexes in the envelope membranes. A component of the translocon in the outer envelope membrane, Toc34, is encoded in Arabidopsis by two homologous genes, atTOC33 and atTOC34. Whereas atTOC34 displays relatively uniform expression throughout development, atTOC33 is strongly upregulated in rapidly growing, photosynthetic tissues. To understand the reason for the existence of these two related genes, we characterized the atTOC33 knockout mutant ppi1. Immunoblotting and proteomics revealed that components of the photosynthetic apparatus are deficient in ppi1 chloroplasts and that nonphotosynthetic chloroplast proteins are unchanged or enriched slightly. Furthermore, DNA array analysis of 3292 transcripts revealed that photosynthetic genes are moderately, but specifically, downregulated in ppi1. Proteome differences in ppi1 could be correlated with protein import rates: ppi1 chloroplasts imported the ribulose-1,5-bisphosphate carboxylase/oxygenase small subunit and 33-kD oxygen-evolving complex precursors at significantly reduced rates, but the import of a 50S ribosomal subunit precursor was largely unaffected. The ppi1 import defect occurred at the level of preprotein binding, which is consistent with a role for atToc33 during preprotein recognition. The data suggest that atToc33 is involved preferentially in the import of photosynthetic proteins and, by extension, that atToc34 is involved in the import of nonphotosynthetic chloroplast proteins.


Subject(s)
Arabidopsis Proteins/genetics , Arabidopsis Proteins/metabolism , Arabidopsis/genetics , Arabidopsis/metabolism , Carrier Proteins/genetics , Carrier Proteins/metabolism , Photosynthetic Reaction Center Complex Proteins/metabolism , Biological Transport, Active , Chloroplasts/genetics , Chloroplasts/metabolism , Down-Regulation , Gene Expression Regulation, Plant , Genes, Plant , Membrane Proteins/genetics , Membrane Proteins/metabolism , Mutation , Photosynthesis/genetics , Plant Proteins/genetics , Plant Proteins/metabolism , RNA, Plant/genetics , RNA, Plant/metabolism
3.
J Biol Chem ; 278(45): 44405-11, 2003 Nov 07.
Article in English | MEDLINE | ID: mdl-12923179

ABSTRACT

Lewy bodies are intracellular fibrillar inclusions composed of alpha-synuclein. They constitute the pathological hallmark of Parkinson's disease, dementia with Lewy bodies, and other neurodegenerative diseases. Although the majority of Lewy bodies are stained for ubiquitin by immunohistochemistry, the substrate for this modification is poorly understood. Insoluble, urea-soluble alpha-synuclein was separated from soluble fractions and subjected to two-dimensional gel electrophoresis to further characterize pathogenic alpha-synuclein species from disease brains. By using this approach, we found that in sporadic Lewy body diseases a highly modified, disease-associated 22-24-kDa alpha-synuclein species is ubiquitinated. Conjugation of one, two, and, to a lesser extent, three ubiquitins was detected. This 22-24-kDa alpha-synuclein species represents partly phosphorylated protein. Furthermore, no generalized impairment of the proteolytic activity of the proteasome was detected in brain regions with Lewy body pathology. Because unmodified alpha-synuclein is degraded by the proteasome in a ubiquitin-independent manner, these data suggest that accumulation of modified 22-24-kDa alpha-synuclein is a disease-specific event which may overwhelm the proteolytic system, leading to aberrant ubiquitination. Accordingly, carboxyl-terminal-truncated alpha-synuclein, presumably the result of aberrant proteolysis, is found only in association with alpha-synuclein aggregates.


Subject(s)
Cysteine Endopeptidases/physiology , Lewy Bodies/metabolism , Multienzyme Complexes/physiology , Nerve Tissue Proteins/metabolism , Parkinson Disease/metabolism , Ubiquitin/metabolism , Aged , Brain/ultrastructure , Cell Fractionation , Glycosylation , Humans , Immunoblotting , Immunohistochemistry , Lewy Bodies/chemistry , Lewy Bodies/pathology , Middle Aged , Molecular Weight , Nerve Tissue Proteins/analysis , Nerve Tissue Proteins/chemistry , Parkinson Disease/pathology , Phosphorylation , Proteasome Endopeptidase Complex , Synucleins , alpha-Synuclein
4.
Curr Opin Chem Biol ; 6(1): 46-50, 2002 Feb.
Article in English | MEDLINE | ID: mdl-11827822

ABSTRACT

A strength of two-dimensional polyacrylamide gel electrophoresis (2D PAGE) is its ability to resolve and investigate the abundance of several thousand proteins in a single sample. This enables identification of the major proteins in a tissue or subcellular fraction by mass spectrometric methods. In addition, 2D PAGE can be used to compare quantities of proteins in related samples, such as those from altered environments or from mutant and wild type, thus allowing the response of classes of proteins to be determined. Those proteins showing a correlated difference in expression may participate in related processes, and this subsequently helps to define protein function. Although there are many limitations of the 2D gel technology that mean it will never be comprehensive in protein coverage, its use for the identification of relatively abundant proteins is now widespread. However, there are still surprisingly few examples of quantitative analysis of changes in protein abundance. In this review we highlight recent advances towards true quantitative analysis of 2D gels that will lead to better prediction of protein function. Despite the development of promising alternatives, 2D PAGE is likely to remain in extensive use for the foreseeable future, because the technology is now simple and readily available to many laboratories.


Subject(s)
Proteins/analysis , Animals , Electrophoresis, Gel, Two-Dimensional/instrumentation , Electrophoresis, Gel, Two-Dimensional/methods , Electrophoresis, Gel, Two-Dimensional/trends , Electrophoresis, Polyacrylamide Gel , Humans , Proteome/analysis , Specimen Handling
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