Literature DB >> 33365719

The complete mitochondrial genome of Sarcophaga caudagalli (Diptera: Sarcophagidae).

Xiao Shen1, Yanjie Shang1, Lipin Ren1, Jifeng Cai1, Yadong Guo1.   

Abstract

Sarcophaga caudagalli belonging to the Sarcophagidae is significant for medical and veterinary management. The complete mitochondrial genome (mitogenome) of S. caudagalli was first sequenced and annotated. The circular molecule was 15,029 bp in length, containing 37 genes (13 protein-coding genes (PCGs), two rRNA genes, 22 tRNA genes, and an A + T-rich region). Phylogenetic analysis showed that the clade of S. caudagalli was clustered separately.
© 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

Entities:  

Keywords:  Mitochondrial genome; Sarcophaga caudagalli; Sarcophagidae

Year:  2019        PMID: 33365719      PMCID: PMC7706462          DOI: 10.1080/23802359.2019.1644552

Source DB:  PubMed          Journal:  Mitochondrial DNA B Resour        ISSN: 2380-2359            Impact factor:   0.658


Among the current number of species of flesh flies, S. caudagalli Bottcher, 1912 is mainly distributed in Asia, such as China, Japan, India, and Thailand, which is an important element of the carrion insect community (Lshijima 1967). The mitogenome has been widely used for phylogeny studies and molecular diagnostics (Shang et al. 2019). In this study, the complete mitogenome of S. caudagalli was 15,029 bp in length (Genbank No. MK820721), containing 37 genes (13 PCGs, two rRNA genes, 22 tRNA genes, and an A + T-rich region). Additionally, it exhibited characteristics of A (39.3%), G (9.6%), C (14.7%), and T (36.4%). Adult specimens of S. caudagalli were captured in December 2018 in Jinghong, Yunnan province, China (21°27′N; 100°25′E). All specimens were frozen to death and stored under −80 °C subsequently. The specimens were identified according to the keys of morphological characteristics (Xu and Zhao 1996). The voucher specimens were assigned a unique field code (CSU19040903) and deposited in the Guo’s Lab (Changsha, Hunan, China). Genomic DNA was extracted using the QIANamp Micro DNA Kit, and then the complete mitogenome was sequenced on an Illumina HiSeq 2500 Platform. Phylogenetic analysis was performed using Neighbour-joining method, and constructed with 13 concatenated PCGs, representing S. caudagalli and 11 other flesh flies. Calliphora pinguis and Chrysomya vomitoria belonging to Calliphoridae were used as an outgroup (Figure 1). The results showed that the clade of S. caudagalli was clustered separately, as well as R. pernix. The complete mitogenome of S. caudagalli provided important information for exploring phylogenetic analysis and population genetics.
Figure 1.

Phylogenetic analysis was performed using Neighbour-joining method, representing S. caudagalli and 11 other flesh flies. Calliphora pinguis and C. vomitoria were used as an outgroup.

Phylogenetic analysis was performed using Neighbour-joining method, representing S. caudagalli and 11 other flesh flies. Calliphora pinguis and C. vomitoria were used as an outgroup.
  1 in total

1.  Comparative Mitogenomic Analysis of Forensically Important Sarcophagid Flies (Diptera: Sarcophagidae) and Implications of Species Identification.

Authors:  Yanjie Shang; Lipin Ren; Wei Chen; Lagabaiyila Zha; Jifeng Cai; Jianan Dong; Yadong Guo
Journal:  J Med Entomol       Date:  2019-02-25       Impact factor: 2.278

  1 in total

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