Information about Stathmin
stathmin 1/oncoprotein 18 | |
| Identifiers | |
| Symbol | STMN1 |
| Alt. Symbols | LAP18 |
| Entrez | 3925 |
| HUGO | 6510 |
| OMIM | 151442 |
| RefSeq | NM_005563 |
| UniProt | P16949 |
| Other data | |
| Locus | Chr. 1 p36.1-35 |
Stathmin is a highly conserved 17kDa protein. Its function as an important regulatory protein of microtubule dynamics has been well characterized. [1] Eukaryotic microtubules are one of three major components of the cell’s cytoskeleton. They are highly dynamic structures that continuously alternate between assembly and disassembly. Stathmin performs an important function in regulating rapid microtubule remodeling of the cytoskeleton in response to the cell’s needs. Microtubules are cylindrical polymers of α,β-tubulin. Their assembly is in part determined by the concentration of free tubulin in the cytoplasm. [2]
At low concentrations of free tubulin, the growth rate at the microtubule ends is slowed and results in an increased rate of depolymerization (disassembly). [3] [1]
Function
Stathmin interacts with two molecules of dimeric α,β-tubulin to form a tight ternary complex called the T2S complex. [1] One mole of stathmin binds to two moles of tubulin dimers through the stathmin-like domain (SLD). [3] When stathmin sequesters tubulin into the T2S complex, tubulin becomes nonpolymerizable. Without tubulin polymerization, there is no microtubule assembly. Through this mechanism, stathmin promotes microtubule disassembly without acting directly on the microtubule ends. [1]The rate of microtubule assembly is an important aspect of cell growth therefore associating regulation of stathmin with cell cycle progress. Regulation of stathmin is cell cycle dependent and controlled by the cell’s protein kinases in response to specific cell signals. [3] [1] Phosphorylation at four serine residues on stathmin named Ser16, Ser25, Ser38 and Ser63 causes weakened stathmin-tubulin binding. Stathmin phosphorylation increases the concentration of tubulin available in the cytoplasm for microtubule assembly. For cells to assemble the mitotic spindle necessary for initiation of the mitotic phase of the cell cycle, stathmin phosphorylation must occur. Without microtuble growth and assembly, the mitotic spindle cannot form, and the cell cycle is arrested. At cytokinesis, the last phase of the cell cycle, rapid dephosphorylation of stathmin occurs to block the cell from entering back into the cell cycle until it is ready. [3]
Oncoprotein Characterization
Stathmin’s role in regulation of the cell cycle causes it to be an oncoprotein named oncoprotein 18 (op18). As op18, stathmin can cause uncontrolled cell proliferation when mutated and not functioning properly. If stathmin is unable to bind to tubulin, it allows for constant microtubule assembly and therefore constant mitotic spindle assembly. With no regulation of the mitotic spindle, the cell cycle is capable of cycling uncontrollably resulting in the unregulated cell growth characteristic of cancer cells. [3]References
1. ^ Jourdain, L., P. Curmi, A. Sobel, D. Pantaloni, and M-F Carlier. Stathmin: A Tubulin-Sequestering Protein Which Forms a Ternary T2S Complex with Two Tubulin Molecules. Biochemistry. 1997. 36: 10817-10821. PMID 9312271
2. ^ Clément, M-J., I. Jourdain, S. Lachkar, P. Savarin, B. Gigant, M. Knossow, F. Toma, A. Sobel, P.A. Curmi. N-Terminal Stathmin-like Peptides Bind Tubulin and Impede Microtubule Assembly. Biochemistry. 2005. 44: 14616-14625. PMID 16262261
3. ^ Cassimeris, L. The oncoprotein 18/stathmin family of microtubule destabilizers. Current Opinion in Cell Biology. 2002. 14: 18-24. PMID 11792540
4. ^ Jourdain, L., P. Curmi, A. Sobel, D. Pantaloni, and M-F Carlier. Stathmin: A Tubulin-Sequestering Protein Which Forms a Ternary T2S Complex with Two Tubulin Molecules. Biochemistry. 1997. 36: 10817-10821. PMID 9312271
5. ^ Jourdain, L., P. Curmi, A. Sobel, D. Pantaloni, and M-F Carlier. Stathmin: A Tubulin-Sequestering Protein Which Forms a Ternary T2S Complex with Two Tubulin Molecules. Biochemistry. 1997. 36: 10817-10821. PMID 9312271
6. ^ Cassimeris, L. The oncoprotein 18/stathmin family of microtubule destabilizers. Current Opinion in Cell Biology. 2002. 14: 18-24. PMID 11792540
7. ^ Jourdain, L., P. Curmi, A. Sobel, D. Pantaloni, and M-F Carlier. Stathmin: A Tubulin-Sequestering Protein Which Forms a Ternary T2S Complex with Two Tubulin Molecules. Biochemistry. 1997. 36: 10817-10821. PMID 9312271
8. ^ Cassimeris, L. The oncoprotein 18/stathmin family of microtubule destabilizers. Current Opinion in Cell Biology. 2002. 14: 18-24. PMID 11792540
9. ^ Jourdain, L., P. Curmi, A. Sobel, D. Pantaloni, and M-F Carlier. Stathmin: A Tubulin-Sequestering Protein Which Forms a Ternary T2S Complex with Two Tubulin Molecules. Biochemistry. 1997. 36: 10817-10821. PMID 9312271
10. ^ Cassimeris, L. The oncoprotein 18/stathmin family of microtubule destabilizers. Current Opinion in Cell Biology. 2002. 14: 18-24. PMID 11792540
11. ^ Cassimeris, L. The oncoprotein 18/stathmin family of microtubule destabilizers. Current Opinion in Cell Biology. 2002. 14: 18-24. PMID 11792540
2. ^ Clément, M-J., I. Jourdain, S. Lachkar, P. Savarin, B. Gigant, M. Knossow, F. Toma, A. Sobel, P.A. Curmi. N-Terminal Stathmin-like Peptides Bind Tubulin and Impede Microtubule Assembly. Biochemistry. 2005. 44: 14616-14625. PMID 16262261
3. ^ Cassimeris, L. The oncoprotein 18/stathmin family of microtubule destabilizers. Current Opinion in Cell Biology. 2002. 14: 18-24. PMID 11792540
4. ^ Jourdain, L., P. Curmi, A. Sobel, D. Pantaloni, and M-F Carlier. Stathmin: A Tubulin-Sequestering Protein Which Forms a Ternary T2S Complex with Two Tubulin Molecules. Biochemistry. 1997. 36: 10817-10821. PMID 9312271
5. ^ Jourdain, L., P. Curmi, A. Sobel, D. Pantaloni, and M-F Carlier. Stathmin: A Tubulin-Sequestering Protein Which Forms a Ternary T2S Complex with Two Tubulin Molecules. Biochemistry. 1997. 36: 10817-10821. PMID 9312271
6. ^ Cassimeris, L. The oncoprotein 18/stathmin family of microtubule destabilizers. Current Opinion in Cell Biology. 2002. 14: 18-24. PMID 11792540
7. ^ Jourdain, L., P. Curmi, A. Sobel, D. Pantaloni, and M-F Carlier. Stathmin: A Tubulin-Sequestering Protein Which Forms a Ternary T2S Complex with Two Tubulin Molecules. Biochemistry. 1997. 36: 10817-10821. PMID 9312271
8. ^ Cassimeris, L. The oncoprotein 18/stathmin family of microtubule destabilizers. Current Opinion in Cell Biology. 2002. 14: 18-24. PMID 11792540
9. ^ Jourdain, L., P. Curmi, A. Sobel, D. Pantaloni, and M-F Carlier. Stathmin: A Tubulin-Sequestering Protein Which Forms a Ternary T2S Complex with Two Tubulin Molecules. Biochemistry. 1997. 36: 10817-10821. PMID 9312271
10. ^ Cassimeris, L. The oncoprotein 18/stathmin family of microtubule destabilizers. Current Opinion in Cell Biology. 2002. 14: 18-24. PMID 11792540
11. ^ Cassimeris, L. The oncoprotein 18/stathmin family of microtubule destabilizers. Current Opinion in Cell Biology. 2002. 14: 18-24. PMID 11792540
External links
Proteins of the cytoskeleton | |
|---|---|
| Microfilaments | Actins - Actin-binding proteins - Actinin - Arp2/3 complex - Cofilin - Destrin - Gelsolin - Myosins - Profilin - Tropomodulin - Troponin (T, C, I) - Tropomyosin - Wiskott-Aldrich syndrome protein |
| Intermediate filaments | type 1 and 2 (Cytokeratin, type I, type II) - type 3 (Desmin, GFAP, Peripherin, Vimentin) - type 4 (Internexin, Nestin, Neurofilament, Synemin, Syncoilin) - type 5 (Lamin A, B) |
| Microtubules | Dyneins - Kinesins - MAPs (Tau protein, Dynamin) - Tubulins - Stathmin |
| Catenins | Alpha catenin - Beta catenin - Plakoglobin (gamma catenin) - Delta catenin |
| Nonhuman | Major sperm proteins - Prokaryotic cytoskeleton (Crescentin, FtsZ, MreB) |
| Other | APC - Dystrophin (Dystroglycan) - plakin (Desmoplakin, Plectin) - Spectrin - Talin - Utrophin - Vinculin |
Oncogenes/Proto-oncogenes | |
|---|---|
| Transcription factors | AP-1 (c-Fos, c-Jun) - c-Myc |
| Tyrosine kinase / Receptors | c-ErbB (HER2/neu, Her 3) - c-Kit - c-Met - c-Ret - Flt3 - |
| Other | c-Akt - c-Bcl-2 - c-Mdm2 - -c-Raf - c-Ras (HRAS) - c-Sis - c-Src - Notch - Stathmin |
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Conservation refers to a high degree of similarity in orthologous DNA sequences, protein sequences, or protein structures amongst various phyla. A highly conserved protein is often related to an important cellular function.
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The unified atomic mass unit (u), or dalton (Da), is a small unit of mass used to express atomic and molecular masses. It is defined to be one twelfth of the mass of an unbound atom of the carbon-12 nuclide, at rest and in its ground state.
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Proteins are large organic compounds made of amino acids arranged in a linear chain and joined together by peptide bonds between the carboxyl and amino groups of adjacent amino acid residues.
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Microtubules are one of the components of the cytoskeleton. They have diameter of ~ 24 nm and length varying from several micrometers to possibly millimeters in axons of nerve cells.
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Microtubules are one of the components of the cytoskeleton. They have diameter of ~ 24 nm and length varying from several micrometers to possibly millimeters in axons of nerve cells.
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cytoskeleton is a cellular "scaffolding" or "skeleton" contained, as all other organelles, within the cytoplasm. It is contained in all eukaryotic cells and recent research has shown it can be present in prokaryotic cells too.
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Identifiers
Symbol TUBA2
Entrez 7278
HUGO 12408
OMIM 602528
RefSeq NM_006001
UniProt Q13748
Other data
Locus Chr. 13 q11 A Tubulin is one of several members of a small family of globular proteins.
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Symbol TUBA2
Entrez 7278
HUGO 12408
OMIM 602528
RefSeq NM_006001
UniProt Q13748
Other data
Locus Chr. 13 q11 A Tubulin is one of several members of a small family of globular proteins.
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Cytoplasm is a gelatinous, semi-transparent fluid that fills most cells. Eukaryotic cells contain a nucleus that is kept separate from the cytoplasm by a double membrane layer. The cytoplasm has three major elements; the cytosol, organelles and inclusions.
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alkene polymerisation, in which each Styrene monomer unit's double bond reforms as a single bond with another styrene monomer and forms polystyrene.]] In polymer chemistry, polymerization
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The cell cycle, or cell-division cycle, is the series of events that take place in a eukaryotic cell leading to its replication. These events can be divided in two broad periods: interphase—during which the cell grows, accumulating nutrients needed for mitosis and
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Phosphorylation is the addition of a phosphate (PO4) group to a protein molecule or a small molecule. Another way to define it would be the introduction of a phosphate group into an organic molecule.
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spindle apparatus is a structure of the eukaryotic cytoskeleton involved in mitosis and meiosis, often referred to as the mitotic spindle during mitosis and the meiotic spindle during meiosis.
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Proteins are large organic compounds made of amino acids arranged in a linear chain and joined together by peptide bonds between the carboxyl and amino groups of adjacent amino acid residues.
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cytoskeleton is a cellular "scaffolding" or "skeleton" contained, as all other organelles, within the cytoplasm. It is contained in all eukaryotic cells and recent research has shown it can be present in prokaryotic cells too.
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Microfilaments are the thinnest filaments of the cytoskeleton found in the cytoplasm of all eukaryotic cells. These linear polymers of actin subunits are flexible and relatively strong, resisting buckling by multi-piconewton compressive forces and filament fracture by nanonewton
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Actin is a globular structural, 42-47 kDa protein found in many eukaryotic cells, with concentrations of over 100 μM. It is also one of the most highly conserved proteins, differing by no more than 5% in species as diverse as algae and humans.
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This is a list of actin-binding proteins in alphabetical order.
List: 0–9 A B C D E F G H I J K L M N O P Q R S T U V W x Y Z
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List: 0–9 A B C D E F G H I J K L M N O P Q R S T U V W x Y Z
References External links
0–9
- 25kDa
- 25kDa ABP from aorta p185neu
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Actinin is a microfilament protein. α-Actinin is necessary for the attachment of actin filaments to the z-line membrane, in muscle cells. The functional protein is an anti-parallel dimer, which cross-links the thin filaments in adjacent sarcomeres, and therefore coordinated
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Arp2/3 complex is a seven-subunit protein that plays a major role in the regulation of the actin cytoskeleton. It is a necessary component of the actin cytoskeleton and is therefore ubiquitous in actin cytoskeleton-containing eukaryotic cells.[1].
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Identifiers
Symbol CFL2
Entrez 1073
HUGO 1875
OMIM 601443
RefSeq NM_021914
UniProt Q9Y281
Other data
Locus Chr. 14 ADF/cofilin is a family of actin-binding proteins which disassembles actin filaments.
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Symbol CFL2
Entrez 1073
HUGO 1875
OMIM 601443
RefSeq NM_021914
UniProt Q9Y281
Other data
Locus Chr. 14 ADF/cofilin is a family of actin-binding proteins which disassembles actin filaments.
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Destrin is a protein in microfilaments.
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External links
- MeSH Destrin
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Gelsolin is an actin-binding protein that is a key regulator of actin filament assembly and disassembly. Gelsolin is one of the most potent members of the actin-severing gelsolin/villin superfamily, as it severs with nearly 100% efficiency.
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Myosins are a large family of motor proteins found in eukaryotic tissues. They are responsible for actin-based motility.
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Structure and Function
Domains
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