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The Saccharomyces c...
The Saccharomyces cerevisiae SOP1 and SOP2 genes, which act in cation homeostasis, can be functionally substituted by the Drosophila lethal(2)giant larvae tumor suppressor gene.
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- Larsson, K (författare)
- Department of Cell and Molecular Biology, Microbiology, Göteborg University, Göteborg, Sweden
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- Böhl, F (författare)
- Department of Developmental Genetics, Deutsches Krebsforschungszentrum, Heidelberg, Germany
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- Sjöström, Ingrid (författare)
- Jönköping University,Tekniska Högskolan,Department of Cell and Molecular Biology, Microbiology, Göteborg University, Göteborg, Sweden
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- Akhtar, N (författare)
- Department of Cell and Molecular Biology, Microbiology, Göteborg University, Göteborg, Sweden
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- Strand, D (författare)
- Department of Developmental Genetics, Deutsches Krebsforschungszentrum, Heidelberg, Germany
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- Mechler, B M (författare)
- Department of Developmental Genetics, Deutsches Krebsforschungszentrum, Heidelberg, Germany
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- Grabowski, R (författare)
- Department of Cell and Molecular Biology, Microbiology, Göteborg University, Göteborg, Sweden
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- Adler, Lennart, 1944 (författare)
- Gothenburg University,Göteborgs universitet,Botaniska institutionen,Botanical Institute,Department of Cell and Molecular Biology, Microbiology, Göteborg University, Göteborg, Sweden
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(creator_code:org_t)
- Elsevier BV, 1998
- 1998
- Engelska.
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Ingår i: The Journal of biological chemistry. - : Elsevier BV. - 0021-9258 .- 1083-351X. ; 273:50, s. 33610-8
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Abstract
Ämnesord
Stäng
- By complementation of a salt-sensitive mutant of Saccharomyces cerevisiae, we cloned the SOP1 gene, encoding a 114.5-kDa protein of 1033 amino acids. Cells deleted for SOP1 exhibited sensitivity to sodium stress, but showed no sensitivity to general osmotic stress. Following exposure of sop1Delta cells to NaCl stress, the intracellular Na+ level and the Na+/K+ ratio rose to values significantly higher than in wild type cells. Deletion of SOP2, encoding a protein sharing 54% amino acid identity with Sop1p, produced only slight Na+ sensitivity. Cells carrying a sop1Deltasop2Delta double deletion became, however, hypersensitive to Na+ and exhibited increased sensitivity also to Li+ and K+, suggesting involvement of both SOP1 and SOP2 in cation homeostasis. The predicted amino acid sequences of Sop1p and Sop2p show significant homologies with the cytoskeletal-associated protein encoded by the Drosophila lethal(2)giant larvae tumor suppressor gene. Immunolocalization of Sop1p revealed a cytoplasmic distribution and cell fractionation studies showed that a significant fraction of Sop1p was recovered in a sedimentable fraction of the cytosolic material. Expression of a Drosophila l(2)gl cDNA in the sop1Deltasop2Delta strain partially restored the Na+ tolerance of the cells, indicating a functional relationship between the Sop proteins and the tumor suppressor protein, and a novel function in cell homeostasis for this family of proteins extending from yeast to human.
Ämnesord
- NATURVETENSKAP -- Biologi (hsv//swe)
- NATURAL SCIENCES -- Biological Sciences (hsv//eng)
- NATURVETENSKAP -- Biologi -- Cellbiologi (hsv//swe)
- NATURAL SCIENCES -- Biological Sciences -- Cell Biology (hsv//eng)
Nyckelord
- Amino Acid Sequence
- Animals
- Base Sequence
- Carrier Proteins
- chemistry
- genetics
- Cytoplasm
- metabolism
- DNA Primers
- Drosophila
- genetics
- Gene Expression Regulation
- Fungal
- Genes
- Tumor Suppressor
- Genetic Complementation Test
- Homeostasis
- Humans
- Molecular Sequence Data
- Mutation
- Saccharomyces cerevisiae
- genetics
- Saccharomyces cerevisiae Proteins
- Sequence Homology
- Amino Acid
- Sodium
- metabolism
- Amino Acid Sequence
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
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