TY - JOUR
T1 - Cloning and sequence analysis of cDNAs encoding precursors of sarafotoxins
T2 - Evidence for an unusual "rosary-type" organization
AU - Ducancel, Frédéric
AU - Matre, Vilborg
AU - Dupont, Christine
AU - Lajeunesse, Evelyne
AU - Wollberg, Zvi
AU - Bdolah, Avner
AU - Kochva, Elazar
AU - Boulain, Jean Claude
AU - Ménez, André
PY - 1993/2/15
Y1 - 1993/2/15
N2 - Sarafotoxins (SRTXs) are 21-amino acid peptides structurally and functionally similar to endothelins (ETs). To understand how SRTXs are overproduced in venom glands of the snakes Atractaspis engaddensis and hence used as toxins, we cloned cDNAs encoding SRTXs and elucidated their nucleotide sequences. We predict that SRTX precursors are large prepropolypeptide chains with an unusual "rosary-type" structure made of 12 successive similar stretches of 40 residues (39 in the first stretch). Each stretch begins with a "spacer" of 19 invariant residues (18 in the first stretch) immediately followed by the sequence of one SRTX isoform. Six different isoforms are identified within a single precursor molecule. Maturation of the precursor may require endopeptidases that cleave the Leu-Cys bond and the Trp-Arg/Lys bond invariably found at the SRTX N and C termini, respectively.
AB - Sarafotoxins (SRTXs) are 21-amino acid peptides structurally and functionally similar to endothelins (ETs). To understand how SRTXs are overproduced in venom glands of the snakes Atractaspis engaddensis and hence used as toxins, we cloned cDNAs encoding SRTXs and elucidated their nucleotide sequences. We predict that SRTX precursors are large prepropolypeptide chains with an unusual "rosary-type" structure made of 12 successive similar stretches of 40 residues (39 in the first stretch). Each stretch begins with a "spacer" of 19 invariant residues (18 in the first stretch) immediately followed by the sequence of one SRTX isoform. Six different isoforms are identified within a single precursor molecule. Maturation of the precursor may require endopeptidases that cleave the Leu-Cys bond and the Trp-Arg/Lys bond invariably found at the SRTX N and C termini, respectively.
UR - http://www.scopus.com/inward/record.url?scp=0027411077&partnerID=8YFLogxK
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AN - SCOPUS:0027411077
SN - 0021-9258
VL - 268
SP - 3052
EP - 3055
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 5
ER -