Evidence map›Paper›PMID 25434036›Full record

ArticleJournal of insect science (Online)2014

Molecular cloning and characterization of a novel P450 gene encoding CYP6BK18 from Dastarcus helophoroides (Coleoptera: Bothrideridae).

Fei-Fei Li, Hai-Dong Wang, Wang Song, Jun Cui, Meng-Lou Li

Abstract read
In one paragraph

Article in Journal of insect science (Online), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Fei-Fei LiCollege of Science, Northwest A&F University, Yangling, Shaanxi 712100, China.
Hai-Dong WangLaboratory of Forestry Pests Biological Control, College of Forestry, Northwest A&F University, Yangling, Shaanxi 712100, China.
Wang SongLaboratory of Forestry Pests Biological Control, College of Forestry, Northwest A&F University, Yangling, Shaanxi 712100, China.
Jun CuiLaboratory of Forestry Pests Biological Control, College of Forestry, Northwest A&F University, Yangling, Shaanxi 712100, China.
Meng-Lou LiLaboratory of Forestry Pests Biological Control, College of Forestry, Northwest A&F University, Yangling, Shaanxi 712100, China limenglou@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A novel cDNA clone encoding a cytochrome P450 gene, named CYP6BK18 (GenBank KC683905), was isolated by reverse transcription PCR from Dastarcus helophoroides (Fairmaire) (Coleoptera: Bothrideridae), a natural enemy of beetles. The full-length cDNA sequence is 1,659 bp, containing a 1,533 bp open reading frame predicting a 510-amino acid protein possessing a transmembrane domain with a calculated molecular weight of 59.4 kDa and a theoretical pI of 8.94. The deduced amino acid sequence of CYP6BK18 showed a 59% identity with CYP6BK17 (GenBank XP_970481.1) from Tribolium castaneum. Phylogenetic analysis indicated that CYP6BK18 was most closely related to CYP6BK17 and CYP6BK14 (GenBank EFA05731.1) from T. castaneum. Expression patterns of CYP6BK18 in different tissues (head, oviduct, midgut, fat bodies, and Malpighian tubules), developmental stages (first- to sixth-instar larvae and adult) and 10 age groups of adult were analyzed by real-time quantitative PCR (RT-qPCR). The results showed that CYP6BK18 was highly expressed in adulthood. Also, RT-qPCR analysis among different age groups of adult showed that CYP6BK18 transcripts were abundant in the spawning period and peaked at the early stage of the adult development. Moreover, the tissue-specific expression levels of CYP6BK18 were in the order of midgut, Malpighian tubes and fatty body from high to low. These results suggest that cytochrome P450 CYP6BK18 may play a role in regulating the development and aging of D. helophoroides.

Indexed as

Amino Acid SequenceAnimalsBase SequenceCloning, MolecularColeopteraCytochrome P-450 Enzyme SystemDNA, ComplementaryInsect ProteinsLarvaMolecular Sequence DataPhylogenyCytochrome P-450 Enzyme SystemDNA, ComplementaryInsect ProteinsagingCYP6 familycytochrome P450Dastarcus helophoroidesmRNA expression

Identifiers

PMID25434036
PMCPMC5633938

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.