Evidence map›Paper›PMID 21978124›Full record

ArticleBMC evolutionary biology2011

Molecular characterization and evolution of a gene family encoding male-specific reproductive proteins in the African malaria vector Anopheles gambiae.

Emiliano Mancini, Francesco Baldini, Federica Tammaro, Maria Calzetta, Aurelio Serrao, Phillip George, Isabelle Morlais, Daniel Masiga, Igor V Sharakhov, David W Rogers and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 25% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 7 institutions in 6 countries.

Emiliano ManciniIstituto-Pasteur - Fondazione Cenci Bolognetti, Dipartimento di Sanità Pubblica e Malattie Infettive, Sapienza Università di Roma, Rome, Italy. emiliano.mancini@uniroma1.it
Francesco Baldini
Federica Tammaro
Maria Calzetta
Aurelio Serrao
Phillip George
Isabelle Morlais
Daniel Masiga
Igor V Sharakhov
David W Rogers
Flaminia Catteruccia
Alessandra della Torre
Istituto Pasteur · ITUniversity of Perugia · ITVirginia Tech · USInternational Centre of Insect Physiology and Ecology · KEMax Planck Institute for Evolutionary Biology · DEOrganisation de Coordination pour la lutte contre les Endémies en Afrique Centrale · CMSapienza University of Rome · IT

Funding

Chromosomal Phylogeny of the Anopheles gambiae ComplexR21AI081023 · NIAID · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI SHARAKHOV, IGOR V · 2009 to 2010
$409k
European Research Council 260897Medical Research Council 78415Medical Research Council G0600062NIAID NIH HHS 5R21AI081023
6 · The paper itself

Abstract

backgroundDuring copulation, the major Afro-tropical malaria vector Anopheles gambiae s.s. transfers male accessory gland (MAG) proteins to females as a solid mass (i.e. the "mating plug"). These proteins are postulated to function as important modulators of female post-mating responses. To understand the role of selective forces underlying the evolution of these proteins in the A. gambiae complex, we carried out an evolutionary analysis of gene sequence and expression divergence on a pair of paralog genes called AgAcp34A-1 and AgAcp34A-2. These encode MAG-specific proteins which, based on homology with Drosophila, have been hypothesized to play a role in sperm viability and function.

resultsGenetic analysis of 6 species of the A. gambiae complex revealed the existence of a third paralog (68-78% of identity), that we named AgAcp34A-3. FISH assays showed that this gene maps in the same division (34A) of chromosome-3R as the other two paralogs. In particular, immuno-fluorescence assays targeting the C-terminals of AgAcp34A-2 and AgAcp34A-3 revealed that these two proteins are localized in the posterior part of the MAG and concentrated at the apical portion of the mating plug. When transferred to females, this part of the plug lies in proximity to the duct connecting the spermatheca to the uterus, suggesting a potential role for these proteins in regulating sperm motility. AgAcp34A-3 is more polymorphic than the other two paralogs, possibly because of relaxation of purifying selection. Since both unequal crossing-over and gene conversion likely homogenized the members of this gene family, the interpretation of the evolutionary patterns is not straightforward. Although several haplotypes of the three paralogs are shared by most A. gambiae s.l. species, some fixed species-specific replacements (mainly placed in the N- and C-terminal portions of the secreted peptides) were also observed, suggesting some lineage-specific adaptation.

conclusionsProgress in understanding the signaling cascade in the A. gambiae reproductive pathway will elucidate the interaction of this MAG-specific protein family with their female counterparts. This knowledge will allow a better evaluation of the relative importance of genes involved in the reproductive isolation and fertility of A. gambiae species and could help the interpretation of the observed evolutionary patterns.

Indexed as

Evolution, MolecularAnimalsAnophelesBayes TheoremBlotting, WesternChromosome MappingComputational BiologyDrosophila ProteinsFemaleHaplotypesInsect HormonesIn Situ Hybridization, FluorescenceIntercellular Signaling Peptides and ProteinsMaleMicroscopy, FluorescenceModels, GeneticDrosophila ProteinsInsect HormonesIntercellular Signaling Peptides and ProteinsPeptidesSP protein, Drosophila

Identifiers

PMID21978124
PMCPMC3199272
OpenAlexW1989413439

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Registered trials

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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.