

FOLLOWUS
1. Key Laboratory of Marine Environment and Ecology Ministry of Education Ocean University of China
2. Third Institute of Oceanography State Oceanic Administration
3. Key Laboratory of Marine Chemistry Theory and Technology Ministry of Education Ocean University of China
网络首发:2011-09-19,
纸质出版:2012
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Cloning, characterization, and expression of Cytochrome b (Cytb)—a key mitochondrial gene from Prorocentrum donghaiense[J]. 海洋湖沼学报(英文), 2012,30(3):424-432.
Zhao, L., Mi, T., Zhen, Y. et al. Cloning, characterization, and expression of Cytochrome b (Cytb)—a key mitochondrial gene from Prorocentrum donghaiense, ., Chin. J. Ocean. Limnol. 30, 424–432 (2012). https://doi.org/10.1007/s00343-012-1137-4
Cloning, characterization, and expression of Cytochrome b (Cytb)—a key mitochondrial gene from Prorocentrum donghaiense[J]. 海洋湖沼学报(英文), 2012,30(3):424-432. DOI: 10.1007/s00343-012-1137-4.
Zhao, L., Mi, T., Zhen, Y. et al. Cloning, characterization, and expression of Cytochrome b (Cytb)—a key mitochondrial gene from Prorocentrum donghaiense, ., Chin. J. Ocean. Limnol. 30, 424–432 (2012). https://doi.org/10.1007/s00343-012-1137-4 DOI:
Mitochondrial cytochrome b (Cytb)
one of the few proteins encoded by the mitochondrial DNA
plays an important role in transferring electrons. As a mitochondrial gene
it has been widely used for phylogenetic analysis. Previously
a 949-bp fragment of the coding gene and mRNA editing were characterized from Prorocentrum donghaiense
which might prove useful for resolving P. donghaiense from closely related species. However
the full-length coding region has not been characterized. In this study
we used rapid amplification of cDNA ends (RACE) to obtain full-length
1 124 bp cDNA. Cytb transcript contained a standard initiation codon ATG
but did not have a recognizable stop codon. Homology comparison showed that the P. donghaiense Cytb had a high sequence identity to Cytb sequences from other dinoflagellate species. Phylogenetic analysis placed Cytb from P. donghaiense in the clade of dinoflagellates and it clustered together strongly with that from P. minimum. Based on the full-length sequence
we inferred 32 editing events at different positions
accounting for 2.93% of the Cytb gene. 34.4% (11) of the changes were A to G
25% (8) were T to C
and 25% (8) were C to U
with smaller proportions of G to C and G to A edits (9.4% (3) and 6.2% (2)
respectively). The expression level of the Cytb transcript was quantified by real-time PCR with a TaqMan probe at different times during the whole growth phase. The average Cytb transcript was present at 39.27±7.46 copies of cDNA per cell during the whole growth cycle
and the expression of Cytb was relatively stable over the different phases. These results deepen our understanding of the structure and characteristics of Cytb in P. donghaiense
and confirmed that Cytb in P. donghaiense is a candidate reference gene for studying the expression of other genes.
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