1989
DOI: 10.1016/0166-6851(89)90102-3
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Cloning and expression of a trypomastigote-specific 85-kilodalton surface antigen gene from Trypanosoma cruzi

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Cited by 27 publications
(16 citation statements)
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“…Other T. cruzi 85-kD surface antigen coding genes have been cloned, and like the SA85-1 genes, they belong to large gene families (19)(20)(21) . These cloned genes do not share significant homology with each other or with SA85-1, indicating that multiple 85-kD families exist, which would further explain the observed surface antigen diversity.…”
Section: Gcg]dggagtgtgcggcctcagtgtggagtatttgcgccctcttccacaccgacactcacmentioning
confidence: 99%
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“…Other T. cruzi 85-kD surface antigen coding genes have been cloned, and like the SA85-1 genes, they belong to large gene families (19)(20)(21) . These cloned genes do not share significant homology with each other or with SA85-1, indicating that multiple 85-kD families exist, which would further explain the observed surface antigen diversity.…”
Section: Gcg]dggagtgtgcggcctcagtgtggagtatttgcgccctcttccacaccgacactcacmentioning
confidence: 99%
“…Several trypomastigote surface antigens have been identified, including those with molecular masses of 90 kD (17), 160 kD (18), and the major 85 kD (9,19,20). A gene encoding an 85-kD surface antigen has been shown to be telomeric (21), and has given rise to speculation about the possibility of antigenic variation in T. cmzi, similar to variant surface glycoprotein (VSG)t switching in African trypanosomes (21).…”
mentioning
confidence: 99%
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“…The major surface glycoproteins of the bloodstream trypomastigote stage of Trypanosoma cruzi are encoded by a large multigene family [1][2][3][4][5][6][7][8][9][10], several members of which are expressed simultaneously and encode glycoproteins of 85-160 kDa. We have previously isolated, characterized, and obtained the complete nucleotide sequence of TSA-1, a surface antigen gene from the Peru strain of T. cruzi belonging to the 85-kDa multigene family [1,2,5].…”
mentioning
confidence: 99%
“…However, the aa sequences downstream of the repeat units in TSA-1 are absent in TSA-S1 with the exception of the 21 amino acid residues immediately upstream of the translational stop site. The COOH terminus of the coding region represents one of the two regions conserved in all 85-kDa multigene family members characterized to date [2][3][4][5][6][7][8] and is the proposed processing site for a phosphatidylinositol linkage [12]. The other conserved region found in all family members examined is a 12-aa region which lies immediately upsteam of the repeat array in TSA-S1 [4,10].…”
mentioning
confidence: 99%