» Articles » PMID: 20102629

Sex and the Single Embryo: Early Deveiopment in the Mediterranean Fruit Fly, Ceratitis Capitata

Overview
Journal BMC Dev Biol
Publisher Biomed Central
Date 2010 Jan 28
PMID 20102629
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

Background: In embryos the maternal-to-zygotic transition (MTZ) integrates post-transcriptional regulation of maternal transcripts with transcriptional activation of the zygotic genome. Although the molecular mechanisms underlying this event are being clarified in Drosophila melanogaster, little is know about the embryogenic processes in other insect species. The recent publication of expressed sequence tags (ESTs) from embryos of the global pest species Ceratitis capitata (medfly) has enabled the investigation of embryogenesis in this species and has allowed a comparison of the embryogenic processes in these two related dipteran species, C. capitata and D. melanogaster, that shared a common ancestor 80-100 mya.

Results: Using a novel PCR-based sexing method, which takes advantage of a putative LTR retrotransposon MITE insertion on the medfly Y chromosome, the transcriptomes of individual early male and female embryos were analysed using RT-PCR. This study is focused on two crucial aspects of the onset of embryonic development: sex determination and cellular blastoderm formation. Together with the three known medfly genes (Cctransformer, Cctransformer2 and Ccdoublesex), the expression patterns of other medfly genes that are similar to the D. melanogaster sex-determination genes (sisterlessA, groucho, deadpan, Sex-lethal, female lethal d, sans fille and intersex) and four cellular blastoderm formation genes (Rho1, spaghetti squash, slow-as-molasses and serendipity-alpha) were analyzed, allowing us to sketch a preliminary outline of the embryonic process in the medfly. Furthermore, a putative homologue of the Zelda gene has been considered, which in D. melanogaster encodes a DNA-binding factor responsible for the maternal-to-zygotic transition.

Conclusions: Our novel sexing method facilitates the study of i) when the MTZ transition occurs in males and females of C. capitata, ii) when and how the maternal information of "female-development" is reprogrammed in the embryos and iii) similarities and differences in the regulation of gene expression in C. capitata and D. melanogaster. We suggest a new model for the onset of the sex determination cascade in the medfly: the maternally inherited Cctra transcripts in the female embryos are insufficient to produce enough active protein to inhibit the male mode of Cctra splicing. The slow rate of development and the inefficiency of the splicing mechanism in the pre-cellular blastoderm facilitates the male-determining factor (M) activity, which probably acts by inhibiting CcTRA protein activity.

Citing Articles

A two-level staging system for the embryonic morphogenesis of the Mediterranean fruit fly (medfly) Ceratitis capitata.

Strobl F, Schmitz A, Schetelig M, Stelzer E PLoS One. 2025; 19(12):e0316391.

PMID: 39774542 PMC: 11684674. DOI: 10.1371/journal.pone.0316391.


Gene drive and genetic sex conversion in the global agricultural pest Ceratitis capitata.

Meccariello A, Hou S, Davydova S, Fawcett J, Siddall A, Leftwich P Nat Commun. 2024; 15(1):372.

PMID: 38191463 PMC: 10774415. DOI: 10.1038/s41467-023-44399-1.


In toto light sheet fluorescence microscopy live imaging datasets of Ceratitis capitata embryonic development.

Strobl F, Schetelig M, Stelzer E Sci Data. 2022; 9(1):340.

PMID: 35705572 PMC: 9200851. DOI: 10.1038/s41597-022-01443-x.


Conditional knockdown of transformer in sheep blow fly suggests a role in repression of dosage compensation and potential for population suppression.

Williamson M, Yan Y, Scott M PLoS Genet. 2021; 17(10):e1009792.

PMID: 34662332 PMC: 8553175. DOI: 10.1371/journal.pgen.1009792.


Nanopore long-read RNA-seq and absolute quantification delineate transcription dynamics in early embryo development of an insect pest.

Bayega A, Oikonomopoulos S, Gregoriou M, Tsoumani K, Giakountis A, Wang Y Sci Rep. 2021; 11(1):7878.

PMID: 33846393 PMC: 8042104. DOI: 10.1038/s41598-021-86753-7.


References
1.
Ruiz M, Milano A, Salvemini M, Eirin-Lopez J, Perondini A, Selivon D . The gene transformer of anastrepha fruit flies (Diptera, tephritidae) and its evolution in insects. PLoS One. 2007; 2(11):e1239. PMC: 2080774. DOI: 10.1371/journal.pone.0001239. View

2.
Rozen S, Skaletsky H . Primer3 on the WWW for general users and for biologist programmers. Methods Mol Biol. 1999; 132:365-86. DOI: 10.1385/1-59259-192-2:365. View

3.
Hempel L, Oliver B . Sex-specific DoublesexM expression in subsets of Drosophila somatic gonad cells. BMC Dev Biol. 2007; 7:113. PMC: 2148063. DOI: 10.1186/1471-213X-7-113. View

4.
Meise M, Hilfiker-Kleiner D, Dubendorfer A, Brunner C, Nothiger R, Bopp D . Sex-lethal, the master sex-determining gene in Drosophila, is not sex-specifically regulated in Musca domestica. Development. 1998; 125(8):1487-94. DOI: 10.1242/dev.125.8.1487. View

5.
Schutt C, Nothiger R . Structure, function and evolution of sex-determining systems in Dipteran insects. Development. 2000; 127(4):667-77. DOI: 10.1242/dev.127.4.667. View