Embryonic toxin expression in the cone snail Conus victoriae: primed to kill or divergent function?
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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Embryonic toxin expression in the cone snail Conus victoriae : primed to kill or divergent function? / Safavi-Hemami, Helena; Siero, William A; Kuang, Zhihe; Williamson, Nicholas A; Karas, John A; Page, Louise R; MacMillan, David; Callaghan, Brid; Kompella, Shiva Nag; Adams, David J; Norton, Raymond S; Purcell, Anthony W.
I: The Journal of Biological Chemistry, Bind 286, Nr. 25, 24.06.2011, s. 22546-57.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Embryonic toxin expression in the cone snail Conus victoriae
T2 - primed to kill or divergent function?
AU - Safavi-Hemami, Helena
AU - Siero, William A
AU - Kuang, Zhihe
AU - Williamson, Nicholas A
AU - Karas, John A
AU - Page, Louise R
AU - MacMillan, David
AU - Callaghan, Brid
AU - Kompella, Shiva Nag
AU - Adams, David J
AU - Norton, Raymond S
AU - Purcell, Anthony W
PY - 2011/6/24
Y1 - 2011/6/24
N2 - Predatory marine cone snails (genus Conus) utilize complex venoms mainly composed of small peptide toxins that target voltage- and ligand-gated ion channels in their prey. Although the venoms of a number of cone snail species have been intensively profiled and functionally characterized, nothing is known about the initiation of venom expression at an early developmental stage. Here, we report on the expression of venom mRNA in embryos of Conus victoriae and the identification of novel α- and O-conotoxin sequences. Embryonic toxin mRNA expression is initiated well before differentiation of the venom gland, the organ of venom biosynthesis. Structural and functional studies revealed that the embryonic α-conotoxins exhibit the same basic three-dimensional structure as the most abundant adult toxin but significantly differ in their neurological targets. Based on these findings, we postulate that the venom repertoire of cone snails undergoes ontogenetic changes most likely reflecting differences in the biotic interactions of these animals with their prey, predators, or competitors. To our knowledge, this is the first study to show toxin mRNA transcripts in embryos, a finding that extends our understanding of the early onset of venom expression in animals and may suggest alternative functions of peptide toxins during development.
AB - Predatory marine cone snails (genus Conus) utilize complex venoms mainly composed of small peptide toxins that target voltage- and ligand-gated ion channels in their prey. Although the venoms of a number of cone snail species have been intensively profiled and functionally characterized, nothing is known about the initiation of venom expression at an early developmental stage. Here, we report on the expression of venom mRNA in embryos of Conus victoriae and the identification of novel α- and O-conotoxin sequences. Embryonic toxin mRNA expression is initiated well before differentiation of the venom gland, the organ of venom biosynthesis. Structural and functional studies revealed that the embryonic α-conotoxins exhibit the same basic three-dimensional structure as the most abundant adult toxin but significantly differ in their neurological targets. Based on these findings, we postulate that the venom repertoire of cone snails undergoes ontogenetic changes most likely reflecting differences in the biotic interactions of these animals with their prey, predators, or competitors. To our knowledge, this is the first study to show toxin mRNA transcripts in embryos, a finding that extends our understanding of the early onset of venom expression in animals and may suggest alternative functions of peptide toxins during development.
KW - Amino Acid Sequence
KW - Animals
KW - Conotoxins/chemistry
KW - Conus Snail/anatomy & histology
KW - Embryo, Nonmammalian/metabolism
KW - Gene Expression Regulation
KW - Mass Spectrometry
KW - Models, Molecular
KW - Molecular Sequence Data
KW - Neurons/metabolism
KW - Peptide Fragments/chemistry
KW - Protein Conformation
KW - RNA, Messenger/genetics
KW - Sequence Alignment
U2 - 10.1074/jbc.M110.217703
DO - 10.1074/jbc.M110.217703
M3 - Journal article
C2 - 21504902
VL - 286
SP - 22546
EP - 22557
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
SN - 0021-9258
IS - 25
ER -
ID: 232825007