scholarly journals Characterization of the EYE2 Gene Required for Eyespot Assembly in Chlamydomonas reinhardtii

Genetics ◽  
2001 ◽  
Vol 158 (3) ◽  
pp. 1037-1049
Author(s):  
Douglas G W Roberts ◽  
Mary Rose Lamb ◽  
Carol L Dieckmann

Abstract The unicellular biflagellate green alga Chlamydomonas reinhardtii can perceive light and respond by altering its swimming behavior. The eyespot is a specialized structure for sensing light, which is assembled de novo at every cell division from components located in two different cellular compartments. Photoreceptors and associated signal transduction components are localized in a discrete patch of the plasma membrane. This patch is tightly packed against an underlying sandwich of chloroplast membranes and carotenoid-filled lipid granules, which aids the cell in distinguishing light direction. In a prior screen for mutant strains with eyespot defects, the EYE2 locus was defined by the single eye2-1 allele. The mutant strain has no eyespot by light microscopy and has no organized carotenoid granule layers as judged by electron microscopy. Here we demonstrate that the eye2-1 mutant is capable of responding to light, although the strain is far less sensitive than wild type to low light intensities and orients imprecisely. Therefore, pigment granule layer assembly in the chloroplast is not required for photoreceptor localization in the plasma membrane. A plasmid-insertion mutagenesis screen yielded the eye2-2 allele, which allowed the isolation and characterization of the EYE2 gene. The EYE2 protein is a member of the thioredoxin superfamily. Site-directed mutagenesis of the active site cysteines demonstrated that EYE2 function in eyespot assembly is redox independent, similar to the auxiliary functions of other thioredoxin family members in protein folding and complex assembly.

1985 ◽  
Vol 7 (3-4) ◽  
pp. 365-373 ◽  
Author(s):  
Sanjay Kumar Mishra ◽  
N. K. Garg ◽  
A. M. Kidwai

1976 ◽  
Vol 13 (5) ◽  
pp. 279-292 ◽  
Author(s):  
Jiann-Wu Wei ◽  
Ronald A. Janis ◽  
Edwin E. Daniel

FEBS Letters ◽  
1985 ◽  
Vol 181 (1) ◽  
pp. 33-38 ◽  
Author(s):  
B. Khalfoun ◽  
D. Degenne ◽  
B. Arbeille-Brassart ◽  
N. Gutman ◽  
P. Bardos

1977 ◽  
Vol 73 (2) ◽  
pp. 382-399 ◽  
Author(s):  
J S Caruthers ◽  
M A Bonneville

The lumenal plasma membrane has been isolated from transitional epithelial cells (urothelium) lining the urinary bladder in sheep by a modified technique involving treatment with hypotonic thioglycolate. The isolated membranes, like those in situ, are distinguished morphologically by arrays of hexagonal particles (in plague regions) separated by smooth interplaque regions. These plaque regions, specifically, can be isolated from the lumenal plasma membrane. Of the proteins constituting the lumenal plasma membrane, five were found to characterize the plaque regions and, in particular, the 33,000-dalton species appears to be most heavily concentrated in the sodium dodecyl sulfate-polyacrylamide gel pattern of the isolated plaque regions. Lipid analyses showed that there are approximately 0.93 mg of phospholipid and 0.27 mg of cholesterol for each milligram of protein, giving a value of 55% lipids and 45% proteins for the composition of the lumenal plasma membrane. The total sialic acid content was measured to be approximately 0.038 micronmol/mg protein for the plasma membrane. Several plasma membrane marker enzymes were found to be associated with the lumenal plasma membrane fraction, but only the 5'-nucleotidase activity was found to be further enriched in the plaque region fraction. Amino acid analysis of the intrinsic proteins of the plaques indicated a polarity index of 45%.


1975 ◽  
Vol 20 (1) ◽  
pp. 99-110 ◽  
Author(s):  
A. Réthy ◽  
A. Trevisani ◽  
R. Manservigi ◽  
V. Tomasi

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