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. 2016 Apr 19;1(1):323–325. doi: 10.1080/23802359.2016.1172045

The complete mitochondrial DNA genome of Chinese Daphnia carinata (Clasocera: Daphniidae)

Xuexia Geng 1,*, Ruixue Cheng 1,*, Daogui Deng 1, Haijun Zhang 1,
PMCID: PMC7871863  PMID: 33644370

Abstract

In this paper, we determined the complete mitochondrial genome of Chinese Daphnia carinata for the first time by the long and accurate polymerase chain reaction and primer-walking methods. It was 15,245 bp in length, with an A + T content of 70.35%, containing 37 typical animal mitochondrial genes and an A + T-rich region. The COI gene started with ACTA. All the 22 typical tRNA genes had a classical cloverleaf structure except for trnS1, in which the D-stem pairings in the DHU arm were absent.

Keywords: Daphnia carinata, Daphnia similoides sinensis, Mitochondrial genome


Water fleas are an important component of the microcrustacean zooplankton, their habitats are mostly continental fresh and saline waters (Forró et al. 2008). Daphnia carinata has become a well-known model species in studying evolutionary biology, environmental biology and ecology (Miner et al. 2013). Only the complete mitochondrial DNA of North American Daphnia pulex (GenBank accession no. AF117817) and the Chinese Daphnia pulex (GenBank accession no. KT003819) and the Chinese Daphnia magna (GenBank accession no. KP296147) have been released in Genbank database. And other partial mitochondrial genome DNA of Daphnia has also been published; however, this is far from enough. Gu et al. (2013) had named Daphnia similoides sinensis for this D. carinata, by comparing the sequences of COI with the similarity of 99%. So the standard of morphology species identification could not meet taxonomy studies. It is, thus, worthy to do the further researches for molecular biology of Daphnia so far, advancing our understanding of Cladoceran diversity and evolution.

Using the long and accurate polymerase chain reaction and primer-walking methods, we sequenced and characterized the complete mitochondrial genome of Chinese D. carinata (sampled from Chaohu, Anhui province in China) for the first time (GenBank accession no. KP721459). The total length is 15,245 bp with an A + T content of 70.35%. Table 1 provides detailed information about the mitogenome. The D. carinata mitogenome including 13 protein-coding genes, 22 transfer RNA genes, two ribosomal RNA genes for the small and large subunits (rrnS and rrnL) and a putative control region. The ATN initiation codon are used in all protein-coding genes except ATP8 (GTG) and COI (ACTA). The TAN termination codon are used in all protein-coding genes except COI, COII, ND4 and ND5 used the incomplete stop codon T. The assignment of incomplete termination codon on these genes could avoid overlapping nucleotides between their adjacent genes (Gong et al. 2012), which is commonly reported in other invertebrates (Masta & Boore 2004). And then they would produce functional stop codons via posttranscriptional polyadenylation (Ojala et al. 1981). Fourteen overlaps were found between adjacent genes (80 bp in total), the longest is 23 bp located rrnL and trnL1; and including eight intergenic spacers ranged from 1 to 30 bp (58 bp in total), of which only two spacer span longer than 10 bp (Figure 1).

Table 1.

Organization of the Chinese Daphnia carinata mitogenome.

No. Gene name Start End Stranda Length Overlap/intergenicb Start codon Stop codon
1 trnI 1 66 J 66      
2 trnQ 121 188 N 68 54    
3 trnM 190 254 J 65 1    
4 ND2 255 1241 J 987   ATG TAG
5 trnW 1240 1303 J 64 −2    
6 trnC 1303 1366 N 64 −1    
7 trnY 1368 1432 N 65 1    
8 COI 1430 2967 J 1538 −3 (A)CTA T––
9 trnL2 2968 3035 J 68      
10 COII 3037 3715 J 679 1 ATG T––
11 trnK 3716 3785 J 70      
12 trnD 3786 3850 J 65      
13 ATP8 3851 4021 J 171   GTG TAG
14 ATP6 4015 4689 J 675 −7 ATG TAA
15 COIII 4689 5477 J 789 −1 ATG TAG
16 trnG 5480 5541 J 62 2    
17 ND3 5542 5895 J 354   ATT TAG
18 trnA 5894 5956 J 63 −2    
19 trnR 5957 6020 J 64      
20 trnN 6021 6087 J 67      
21 trnS1 6088 6152 J 65      
22 trnE 6153 6217 J 65      
23 trnF 6217 6280 N 64 −1    
24 ND5 6281 7994 N 1714   ATA T––
25 trnH 7989 8051 N 63 −6    
26 ND4 8052 9369 N 1318 1 ATG T––
27 ND4L 9369 9647 N 279 −1 ATT TAA
28 trnT 9678 9740 J 63 30    
29 trnP 9741 9804 N 64      
30 ND6 9822 10,313 J 492 17 ATT TAA
31 Cytb 10,313 11,446 J 1134 −1 ATG TAG
32 trnS2 11,446 11,514 J 69 −1    
33 ND1 11,505 12,440 N 936 −10 ATG TAA
34 trnL1 12,444 12,510 N 67 3    
35 rrnL 12,488 13,849 N 1362 −23    
36 trnV 13,828 13,899 N 72 −22    
37 rrnS 13,898 14,644 N 747 −2    
38 D-loop 14,644 15,245 J 601      
a

J and N refer to the majority and the minority strand, respectively.

b

Positive numbers indicate the number of intergenic nucleotides. Negative numbers indicate that adjacent genes overlap.

Figure 1.

Figure 1.

Phylogenetic tree obtained by the maximum-likelihood (ML) method based on amino acid sequences of ND5 gene.

All 22 tRNA genes are ranged from 62 bp to 72 bp in size, showing the typical cloverleaf secondary structures except for trnS1, in which its DHU arm simply formed a loop. Generally speaking, the aberrant loop in trnS is a common theme in metazoan mitochondrial genomes. Whether or not the aberrant tRNAs lose their respective functions is still unknown, however, these shortage may be modified by RNA-editing mechanisms (Masta & Boore 2004; Li et al. 2012). The rrnL and rrnS are 1362 bp and 747 bp, respectively. The rRNA genes with A + T content of 72.69%.

The putative control region is located between rrnS and trnI with a sequenced length of 601 bp, with the A + T content of 72.54%. This region was usually believed to play an important role in the transcription and replication of mitogenome (Clayton 1992; Delarbre et al. 2001; Delport et al. 2002; Yu et al. 2013).

The complete mitogenome of the Chinese Daphina carinata reported here is expected to supply more molecular information for further studies of the daphnia phylogeny and for analyses on the taxonomic status of the Cladocera.

Acknowledgments

Disclosure statement

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.

Funding information

This work was supported by the National Natural Science Foundation of China (81272377 and 31370470), the Natural Science Foundation of Anhui Province of China (1208085MC45) and the open-ended fund of Anhui Key Laboratory of Plant Resources and Biology (ZYZWSW2014014).

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