TY - JOUR
T1 - Cloning, expression and localization of the Daphnia carinata transformer gene DcarTra during different reproductive stages
AU - Kong, Ling
AU - Lv, Weiwei
AU - Huang, Youhui
AU - Liu, Zhiquan
AU - Yang, Yang
AU - Zhao, Yunlong
N1 - Publisher Copyright:
© 2015 Elsevier B.V.
PY - 2015/7/25
Y1 - 2015/7/25
N2 - In this study, the full-length cDNA of the Transformer (. Tra) gene from the common freshwater species Daphnia carinata (. DcarTra; GenBank accession no. KJ735445) was cloned using primers based on homologous sequences and rapid amplification of cDNA ends (RACE). The relative expression and localization of DcarTra and the cellular abundance of the DcarTra protein during different sexual phases were subsequently investigated. The full-length DcarTra cDNA was 1620. bp with an ORF of 1143. bp encoding a 380 amino acid polypeptide. Phylogenetic analysis identified closely related genes in Daphnia magna and Daphnia pulex, and more distantly related genes in other insects. Quantitative PCR showed that DcarTra expression was highest in males, followed by sexual females, and lowest in parthenogenetic females. Whole-mount in situ hybridization showed that DcarTra was mainly expressed in the thoracic limbs, ovaries and rectum in parthenogenetic females, and in the joints of second antennae, ovaries, rectum and ventral processes in sexual females. Western blotting showed two differently phosphorylated forms of the Tra protein. When Tra is phosphorylated, DcarTra protein levels were much higher in males than in two females. Otherwise, when Tra is dephosphorylated, the highest Tra protein levels were in sexual females, which revealed that D. carinata can control the sexual transition via these two forms. Together these results suggest that DcarTra plays significant roles in the reproductive transformation of D. carinata and dephosphorylation of DcarTra may be the trigger for females to transform into males.
AB - In this study, the full-length cDNA of the Transformer (. Tra) gene from the common freshwater species Daphnia carinata (. DcarTra; GenBank accession no. KJ735445) was cloned using primers based on homologous sequences and rapid amplification of cDNA ends (RACE). The relative expression and localization of DcarTra and the cellular abundance of the DcarTra protein during different sexual phases were subsequently investigated. The full-length DcarTra cDNA was 1620. bp with an ORF of 1143. bp encoding a 380 amino acid polypeptide. Phylogenetic analysis identified closely related genes in Daphnia magna and Daphnia pulex, and more distantly related genes in other insects. Quantitative PCR showed that DcarTra expression was highest in males, followed by sexual females, and lowest in parthenogenetic females. Whole-mount in situ hybridization showed that DcarTra was mainly expressed in the thoracic limbs, ovaries and rectum in parthenogenetic females, and in the joints of second antennae, ovaries, rectum and ventral processes in sexual females. Western blotting showed two differently phosphorylated forms of the Tra protein. When Tra is phosphorylated, DcarTra protein levels were much higher in males than in two females. Otherwise, when Tra is dephosphorylated, the highest Tra protein levels were in sexual females, which revealed that D. carinata can control the sexual transition via these two forms. Together these results suggest that DcarTra plays significant roles in the reproductive transformation of D. carinata and dephosphorylation of DcarTra may be the trigger for females to transform into males.
KW - ISH: in situ hybridization
KW - ORF: the open reading frame
KW - QPCR real time PCR UTR untranslated region
KW - RACE-PCR: rapid amplification of cDNA ends-- Polymerase chain reaction
UR - https://www.scopus.com/pages/publications/84929946235
U2 - 10.1016/j.gene.2015.04.057
DO - 10.1016/j.gene.2015.04.057
M3 - 文章
C2 - 25917617
AN - SCOPUS:84929946235
SN - 0378-1119
VL - 566
SP - 248
EP - 256
JO - Gene
JF - Gene
IS - 2
ER -