TY - JOUR
T1 - Protein expression during the embryonic development of a gastropod
AU - Sun, Jin
AU - Zhang, Yu
AU - Thiyagarajan, Vengatesen
AU - Qian, Pei Yuan
AU - Qiu, Jian Wen
N1 - This study was supported by a HKBU postgraduate scholarship to J. S., a grant (HKBU FRG/08-09/II-08) to J. W. Q., and a grant (AoE/P-04/04-2-II) to P. Y. Q.
PY - 2010/7
Y1 - 2010/7
N2 - Despite the potential use of gastropod embryos in basic and applied research, little is known about their protein expression. We examined, for the first time, changes in proteomic profile during embryonic development of Pomacea canaliculata from an embryo without a shell (stage II) to an embryo with a fully formed shell (stage III) to understand the roles that proteins play in critical developmental events, such as the formation of shell, operculum and heart, and the differentiation of head and foot. To analyze protein expression during development, we used 2-DE to detect, MS to analyze, and de novo peptide sequencing followed by MS-BLAST to identify the proteins. The de novo cross-species protein identification method was adopted because of a lack of genomic and proteomic data in the whole class of Gastropoda. 2-DE detected approximately 700 protein spots. Among the 125 spots that were abundant, 52% were identified, a marked improvement over the conventional direct MS-BLAST method. These proteins function in perivitelline fluid utilization, shell formation, protein synthesis and folding, and cell cycle and cell fate determination, providing evidence to support that this embryonic period is a period of dynamic protein synthesis and metabolism. The data shall provide a basis for further studies of how gastropod embryos respond to natural and human-induced changes in the environment.
AB - Despite the potential use of gastropod embryos in basic and applied research, little is known about their protein expression. We examined, for the first time, changes in proteomic profile during embryonic development of Pomacea canaliculata from an embryo without a shell (stage II) to an embryo with a fully formed shell (stage III) to understand the roles that proteins play in critical developmental events, such as the formation of shell, operculum and heart, and the differentiation of head and foot. To analyze protein expression during development, we used 2-DE to detect, MS to analyze, and de novo peptide sequencing followed by MS-BLAST to identify the proteins. The de novo cross-species protein identification method was adopted because of a lack of genomic and proteomic data in the whole class of Gastropoda. 2-DE detected approximately 700 protein spots. Among the 125 spots that were abundant, 52% were identified, a marked improvement over the conventional direct MS-BLAST method. These proteins function in perivitelline fluid utilization, shell formation, protein synthesis and folding, and cell cycle and cell fate determination, providing evidence to support that this embryonic period is a period of dynamic protein synthesis and metabolism. The data shall provide a basis for further studies of how gastropod embryos respond to natural and human-induced changes in the environment.
KW - 2-DE
KW - Animal proteomics
KW - Apple snail
KW - de novo sequencing
KW - Embryonic development
KW - Gastropod
UR - https://www.scopus.com/pages/publications/77954709515
U2 - 10.1002/pmic.200900846
DO - 10.1002/pmic.200900846
M3 - Journal article
C2 - 20455212
AN - SCOPUS:77954709515
SN - 1615-9853
VL - 10
SP - 2701
EP - 2711
JO - Proteomics
JF - Proteomics
IS - 14
ER -