Highly conserved amino-acid sequence between murine STAT3 and a revised human STAT3 sequence
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Della Pietra, L
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Ist Ricerca Cesare Serono, Drug Discovery Dept, I-00040 Ardea, Rome, ItalyIst Ricerca Cesare Serono, Drug Discovery Dept, I-00040 Ardea, Rome, Italy
Della Pietra, L
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Bressan, A
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Ist Ricerca Cesare Serono, Drug Discovery Dept, I-00040 Ardea, Rome, ItalyIst Ricerca Cesare Serono, Drug Discovery Dept, I-00040 Ardea, Rome, Italy
Bressan, A
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Pezzotti, AR
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Ist Ricerca Cesare Serono, Drug Discovery Dept, I-00040 Ardea, Rome, ItalyIst Ricerca Cesare Serono, Drug Discovery Dept, I-00040 Ardea, Rome, Italy
Pezzotti, AR
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Serlupi-Crescenzi, O
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Ist Ricerca Cesare Serono, Drug Discovery Dept, I-00040 Ardea, Rome, ItalyIst Ricerca Cesare Serono, Drug Discovery Dept, I-00040 Ardea, Rome, Italy
Serlupi-Crescenzi, O
[1
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[1] Ist Ricerca Cesare Serono, Drug Discovery Dept, I-00040 Ardea, Rome, Italy
Signal transducer and activator of transcription 3 (STAT3) is an important mediator of cytokine signaling, whose cDNA and protein sequences have been fully characterized. We sequenced the whole human STAT3 cDNA isolated from HepG2 cells. The new sequence determined contains 43 nucleotide changes overall, corresponding to six modifications at the amino-acid level. The revised amino-acid sequence of human STAT3 is now completely identical to the mouse sequence, except for a single amino-acid change at position 760. Thus STAT3 now results as one of the most evolutionarily conserved among known proteins. By using specific RT-PCR we could discriminate between the original sequence and the new variant. Amplification of regions within the src-homology domain 2 (SH2) of STAT3, from the RNAs of 11 different tissues or cells, revealed only the expression of the new SH2 variant. Besides, only this SH2 variant was amplified from human genomic DNA. We conclude that the new sequence we have determined in this study represents a revised sequence of hSTAT3 or, less likely, a new predominant allele. (C) 1998 Elsevier Science B.V. All rights reserved.
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Technion Israel Inst Technol, Fac Biol, Emerson Bldg, Haifa, IsraelTechnion Israel Inst Technol, Fac Biol, Emerson Bldg, Haifa, Israel
Argoetti, Amir
Shalev, Dor
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Technion Israel Inst Technol, Fac Biol, Emerson Bldg, Haifa, IsraelTechnion Israel Inst Technol, Fac Biol, Emerson Bldg, Haifa, Israel
Shalev, Dor
Polyak, Galia
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Technion Israel Inst Technol, Fac Biol, Emerson Bldg, Haifa, IsraelTechnion Israel Inst Technol, Fac Biol, Emerson Bldg, Haifa, Israel
Polyak, Galia
Shima, Noa
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Technion Israel Inst Technol, Fac Biol, Emerson Bldg, Haifa, IsraelTechnion Israel Inst Technol, Fac Biol, Emerson Bldg, Haifa, Israel
Shima, Noa
Biran, Hadas
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Technion Israel Inst Technol, Fac Comp Sci, Taub Bldg, Haifa, IsraelTechnion Israel Inst Technol, Fac Biol, Emerson Bldg, Haifa, Israel
Biran, Hadas
Lahav, Tamar
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Technion Israel Inst Technol, Fac Biol, Emerson Bldg, Haifa, IsraelTechnion Israel Inst Technol, Fac Biol, Emerson Bldg, Haifa, Israel
Lahav, Tamar
Hashimshony, Tamar
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Technion Israel Inst Technol, Fac Biol, Emerson Bldg, Haifa, IsraelTechnion Israel Inst Technol, Fac Biol, Emerson Bldg, Haifa, Israel
Hashimshony, Tamar
Mandel-Gutfreund, Yael
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Technion Israel Inst Technol, Fac Biol, Emerson Bldg, Haifa, Israel
Technion Israel Inst Technol, Fac Comp Sci, Taub Bldg, Haifa, IsraelTechnion Israel Inst Technol, Fac Biol, Emerson Bldg, Haifa, Israel