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The study of the transformer gene from Bactrocera dorsalis and B. correcta with putative core promoter regions

BACKGROUND: The transformer (tra) is a sex determining switch in different orders of insects, including Diptera, as in the family Tephritidae. The lifelong autoregulatory loop of tra female-specific splicing can be reset by the intervention of male-specific primary signals (M factor). In early devel...

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Autores principales: Laohakieat, Kamoltip, Aketarawong, Nidchaya, Isasawin, Siriwan, Thitamadee, Siripong, Thanaphum, Sujinda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736151/
https://www.ncbi.nlm.nih.gov/pubmed/26833079
http://dx.doi.org/10.1186/s12863-016-0342-0
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author Laohakieat, Kamoltip
Aketarawong, Nidchaya
Isasawin, Siriwan
Thitamadee, Siripong
Thanaphum, Sujinda
author_facet Laohakieat, Kamoltip
Aketarawong, Nidchaya
Isasawin, Siriwan
Thitamadee, Siripong
Thanaphum, Sujinda
author_sort Laohakieat, Kamoltip
collection PubMed
description BACKGROUND: The transformer (tra) is a sex determining switch in different orders of insects, including Diptera, as in the family Tephritidae. The lifelong autoregulatory loop of tra female-specific splicing can be reset by the intervention of male-specific primary signals (M factor). In early development, the functional female and truncated male TRA proteins relay the sexual fates to the alternative splicing of a bisexual switch gene, doublesex (dsx) cascading the sexual differentiation processes. Bactrocera dorsalis (Hendel) and Bactrocera correcta (Bezzi) are among the Bactrocera model worldwide key pests. Area-wide integrated pest management using the male-only Sterile Insect Technique (SIT) relying on genetic sexing systems is effective in control programs. We undertook the molecular characterization and comparative studies of the tra orthologues in the Bactrocera species, including the Salaya1 genetic sexing strain (GSS). RESULTS: RT-PCR revealed that B. dorsalis tra (Bdtra) and B. correcta tra (Bctra) transcripts contained conservation of both constitutive exons and male-specific exons as in other Bactrocera. However, new Bdtra male-specific exons were retained, diversifying the pattern of the male-specifically spliced transcripts. The coding sequences of tra were highly conserved in Bactrocera (86–95 %) but less so among related genera (61–65 %) within the same Tephritidae family. A conservation of deduced amino acid sequences (18 residues), called the TEP region, was identified to be distinctive among tephritids. The 5’ regulatory sequence containing many structural characteristics of the putative core promoter was discovered in B. correcta. The expression patterns of Bdtra and Bctra were sex-specifically spliced and the signals relayed to the dsx genes in the adult wild-types. However, the coexistence of male- and female-specifically spliced transcripts (980 and 626 bp, respectively) of the B. dorsalis wild-type strain was found in the Salaya1 GSS adult males. The Bdtra RNA interference masculinized the XX karyotype females into pseudomales, but their testes were mostly not well developed. CONCLUSIONS: Bdtra and Bctra have sex-specific splicing, similar to Bactroceras, Ceratitis capitata (Wiedemann), and Anastrephas. A newly identified TEP region is proposed in tephritids. A putative core promoter has been discovered in Bctra. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12863-016-0342-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-47361512016-02-03 The study of the transformer gene from Bactrocera dorsalis and B. correcta with putative core promoter regions Laohakieat, Kamoltip Aketarawong, Nidchaya Isasawin, Siriwan Thitamadee, Siripong Thanaphum, Sujinda BMC Genet Research Article BACKGROUND: The transformer (tra) is a sex determining switch in different orders of insects, including Diptera, as in the family Tephritidae. The lifelong autoregulatory loop of tra female-specific splicing can be reset by the intervention of male-specific primary signals (M factor). In early development, the functional female and truncated male TRA proteins relay the sexual fates to the alternative splicing of a bisexual switch gene, doublesex (dsx) cascading the sexual differentiation processes. Bactrocera dorsalis (Hendel) and Bactrocera correcta (Bezzi) are among the Bactrocera model worldwide key pests. Area-wide integrated pest management using the male-only Sterile Insect Technique (SIT) relying on genetic sexing systems is effective in control programs. We undertook the molecular characterization and comparative studies of the tra orthologues in the Bactrocera species, including the Salaya1 genetic sexing strain (GSS). RESULTS: RT-PCR revealed that B. dorsalis tra (Bdtra) and B. correcta tra (Bctra) transcripts contained conservation of both constitutive exons and male-specific exons as in other Bactrocera. However, new Bdtra male-specific exons were retained, diversifying the pattern of the male-specifically spliced transcripts. The coding sequences of tra were highly conserved in Bactrocera (86–95 %) but less so among related genera (61–65 %) within the same Tephritidae family. A conservation of deduced amino acid sequences (18 residues), called the TEP region, was identified to be distinctive among tephritids. The 5’ regulatory sequence containing many structural characteristics of the putative core promoter was discovered in B. correcta. The expression patterns of Bdtra and Bctra were sex-specifically spliced and the signals relayed to the dsx genes in the adult wild-types. However, the coexistence of male- and female-specifically spliced transcripts (980 and 626 bp, respectively) of the B. dorsalis wild-type strain was found in the Salaya1 GSS adult males. The Bdtra RNA interference masculinized the XX karyotype females into pseudomales, but their testes were mostly not well developed. CONCLUSIONS: Bdtra and Bctra have sex-specific splicing, similar to Bactroceras, Ceratitis capitata (Wiedemann), and Anastrephas. A newly identified TEP region is proposed in tephritids. A putative core promoter has been discovered in Bctra. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12863-016-0342-0) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-01 /pmc/articles/PMC4736151/ /pubmed/26833079 http://dx.doi.org/10.1186/s12863-016-0342-0 Text en © Laohakieat et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Laohakieat, Kamoltip
Aketarawong, Nidchaya
Isasawin, Siriwan
Thitamadee, Siripong
Thanaphum, Sujinda
The study of the transformer gene from Bactrocera dorsalis and B. correcta with putative core promoter regions
title The study of the transformer gene from Bactrocera dorsalis and B. correcta with putative core promoter regions
title_full The study of the transformer gene from Bactrocera dorsalis and B. correcta with putative core promoter regions
title_fullStr The study of the transformer gene from Bactrocera dorsalis and B. correcta with putative core promoter regions
title_full_unstemmed The study of the transformer gene from Bactrocera dorsalis and B. correcta with putative core promoter regions
title_short The study of the transformer gene from Bactrocera dorsalis and B. correcta with putative core promoter regions
title_sort study of the transformer gene from bactrocera dorsalis and b. correcta with putative core promoter regions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736151/
https://www.ncbi.nlm.nih.gov/pubmed/26833079
http://dx.doi.org/10.1186/s12863-016-0342-0
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