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1.
Genome Biol Evol ; 4(2): 155-67, 2012.
Article in English | MEDLINE | ID: mdl-22215803

ABSTRACT

In theory, the loss of sexual reproduction is expected to result in the accumulation of deleterious mutations. In aphids, two main types of life cycle, cyclic and obligate parthenogenesis, represent respectively "sexual" and "asexual" reproductive modes. We used the complete pea aphid genome and previously published expressed sequence tags (ESTs) from two other aphid species. In addition, we obtained 100,000 new ESTs from five more species. The final set comprised four sexual and four asexual aphid species and served to test the influence of the reproductive mode on the evolutionary rates of genes. We reconstructed coding sequences from ESTs and annotated these genes, discovering a novel peptide gene family that appears to be among the most highly expressed transcripts from several aphid species. From 203 genes found to be 1:1 orthologs among the eight species considered, we established a species tree that partly conflicted with taxonomy (for Myzus ascalonicus). We then used this topology to evaluate the dynamics of evolutionary rates and mutation accumulation in the four sexual and four asexual taxa. No significant increase of the nonsynonymous to synonymous ratio or of nonsynonymous mutation numbers was found in any of the four branches for asexual taxa. We however found a significant increase of the synonymous rate in the branch leading to the asexual species Rhopalosiphum maidis, which could be due to a change in the mutation rate or to an increased number of generations implied by its change of life cycle.


Subject(s)
Aphids/genetics , Evolution, Molecular , Genes, Insect/genetics , Animals , Expressed Sequence Tags , Gene Dosage/genetics , Likelihood Functions , Mitochondrial Proteins/genetics , Molecular Sequence Annotation , Molecular Sequence Data , Open Reading Frames/genetics , Phylogeny , RNA, Messenger/genetics , RNA, Messenger/metabolism , Reproduction/genetics , Species Specificity
2.
Insect Mol Biol ; 19 Suppl 2: 87-95, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20482642

ABSTRACT

Aphids respond to environmental changes by developing alternative phenotypes with differing reproductive modes. Parthenogenetic reproduction occurs in spring and summer, whereas decreasing day lengths in autumn provoke the production of sexual forms. Changing environmental signals are relayed by brain neuroendocrine signals to the ovarioles. We combined bioinformatic analyses with brain peptidomics and cDNA analyses to establish a catalogue of pea aphid neuropeptides and neurohormones. 42 genes encoding neuropeptides and neurohormones were identified, of which several were supported by expressed sequence tags and/or peptide mass analyses. Interesting features of the pea aphid peptidome are the absence of genes coding for corazonin, vasopressin and sulfakinin and the presence of 10 different genes coding insulin related peptides, one of which appears to be very abundantly expressed.


Subject(s)
Aphids/genetics , Aphids/metabolism , Insect Hormones/genetics , Insect Hormones/metabolism , Insect Proteins/genetics , Insect Proteins/metabolism , Neuropeptides/genetics , Neuropeptides/metabolism , Neurotransmitter Agents/genetics , Neurotransmitter Agents/metabolism , Amino Acid Sequence , Animals , DNA, Complementary/genetics , Expressed Sequence Tags , Gene Library , Genes, Insect , Molecular Sequence Data , Pisum sativum/parasitology , Phenotype , Photoperiod , Protein Precursors/genetics , Protein Precursors/metabolism , Proteome , Sequence Homology, Amino Acid , Signal Transduction , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
3.
BMC Genomics ; 10: 456, 2009 Sep 29.
Article in English | MEDLINE | ID: mdl-19788735

ABSTRACT

BACKGROUND: Aphid adaptation to harsh winter conditions is illustrated by an alternation of their reproductive mode. Aphids detect photoperiod shortening by sensing the length of the night and switch from viviparous parthenogenesis in spring and summer, to oviparous sexual reproduction in autumn. The photoperiodic signal is transduced from the head to the reproductive tract to change the fate of the future oocytes from mitotic diploid embryogenesis to haploid formation of gametes. This process takes place in three consecutive generations due to viviparous parthenogenesis. To understand the molecular basis of the switch in the reproductive mode, transcriptomic and proteomic approaches were used to detect significantly regulated transcripts and polypeptides in the heads of the pea aphid Acyrthosiphon pisum. RESULTS: The transcriptomic profiles of the heads of the first generation were slightly affected by photoperiod shortening. This suggests that trans-generation signalling between the grand-mothers and the viviparous embryos they contain is not essential. By analogy, many of the genes and some of the proteins regulated in the heads of the second generation are implicated in visual functions, photoreception and cuticle structure. The modification of the cuticle could be accompanied by a down-regulation of the N-beta-alanyldopamine pathway and desclerotization. In Drosophila, modification of the insulin pathway could cause a decrease of juvenile hormones in short-day reared aphids. CONCLUSION: This work led to the construction of hypotheses for photoperiodic regulation of the switch of the reproductive mode in aphids.


Subject(s)
Aphids/genetics , Gene Expression Profiling , Photoperiod , Proteome/metabolism , Seasons , Adaptation, Physiological/genetics , Animals , Aphids/metabolism , Aphids/physiology , Dopamine/analogs & derivatives , Dopamine/metabolism , Down-Regulation , Female , Genes, Insect , Head , Oligonucleotide Array Sequence Analysis , Parthenogenesis/genetics
4.
Insect Biochem Mol Biol ; 37(10): 1094-102, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17785197

ABSTRACT

Seasonal photoperiodism in aphids is responsible for the spectacular switch from asexual to sexual reproduction. However, little is known on the molecular and physiological mechanisms involved in reproductive mode shift through the action of day length. Earlier works showed that aphid head, but not eyes, directly perceives the photoperiodic signal through the cuticle. In order to identify genes regulating the photoperiodic response, a 3321 cDNA microarray developed for the pea aphid, Acyrthosiphon pisum was used to compare RNA populations extracted from heads of short- and long-day reared aphids. Microarray analyses revealed that 59 different transcripts were significantly regulated, among which a majority encoded cuticular proteins and several encoded proteins involved in cellular signalling or signal transduction. These results were confirmed by quantitative RT-PCR experiments on two cuticular and three signalling protein genes. Complementary experiments eliminated moulting and circadian rhythms as putative confounding effects. Quantitative RT-PCR performed at additional developmental stages demonstrated the regulation of expression of cuticular and signalling protein genes during the whole process of photoperiod shortening. This suggests that photoperiodic changes could affect cuticle structure and cell to cell communication in the head of aphids in relation with the switch of reproductive modes.


Subject(s)
Aphids/genetics , Gene Expression Regulation/radiation effects , Insect Proteins/genetics , Photoperiod , Seasons , Animals , Aphids/growth & development , Aphids/radiation effects , Female , Gene Expression Profiling , Head , Insect Proteins/metabolism , Male , Oligonucleotide Array Sequence Analysis , RNA, Messenger/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Signal Transduction/radiation effects
5.
Heredity (Edinb) ; 95(1): 24-33, 2005 Jul.
Article in English | MEDLINE | ID: mdl-15931255

ABSTRACT

In Chile, the aphid Sitobion avenae is of recent introduction, lives on cultivated and wild Poaceae, and is thought to reproduce by permanent parthenogenesis. In order to study the genetic variability and population structure of this species, five microsatellite loci were typed from individual aphids collected from different cultivated and wild host plants, from different geographical zones, and years. Chilean populations showed a high degree of heterozygosity and a low genetic variability across regions and years, with four predominant genotypes representing nearly 90% of the sample. This pattern of low clonal diversity and high heterozygosity was interpreted as the result of recent founder events from a few asexually reproducing genotypes. Most geographical and temporal variation observed in the genetic composition resulted from fluctuations of a few predominant clones. In addition, comparisons of the genotypes found in Chile with those described in earlier surveys of S. avenae populations in Western Europe led us to identify 'superclones' with large geographical distribution and high ecological success, and to make a preliminary exploration of the putative origin(s) of S. avenae individuals introduced to Chile.


Subject(s)
Aphids/genetics , Genetics, Population , Parthenogenesis , Agriculture , Animals , Chile , Clone Cells , Geography , Microsatellite Repeats , Pest Control , Plants, Edible , Poaceae
6.
Mol Ecol ; 14(1): 325-36, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15643974

ABSTRACT

Cyclically parthenogenetic organisms may have facultative asexual counterparts. Such organisms, including aphids, are therefore interesting models for the study of ecological and genetic interactions between lineages differing in reproductive mode. Earlier studies on aphids have revealed major differences in the genetic outcomes of populations that are possibly resulting mostly either from sexual or from asexual reproduction. Besides, notable gene flow between sexual and asexual derivatives has been suspected, which could lead to the emergence of new asexual lineages. The present study examines the interplay between these lineages and is based on analyses of population structure of individuals that may contribute to the pool of sexual reproductive forms in the host alternating aphid Rhopalosiphum padi. Using a Bayesian assignment method, we first show that the sexual forms of R. padi on mating sites encompass two genetically distinct clusters of individuals in the western part of France. The first cluster included unique genotypes of sexual lineages, while the second cluster included facultatively asexual lineages in numerous copies, the reproductive mode of the two clusters being confirmed by reference clones. Sexual reproductive forms produced by sexual and facultatively asexual lineages are thus admixed at mating sites which gives a large opportunity for the two clusters to mate with each other. Nevertheless, this study also highlights, as previously demonstrated, that the two clusters retained high genetic differentiation. Possible explanations for the inferred limited genetic exchanges are advanced in the discussion, but further dedicated investigations are required to solve this paradox.


Subject(s)
Aphids/physiology , Parthenogenesis/physiology , Reproduction/physiology , Animals , Aphids/genetics , Chromosome Mapping , Demography , Female , France , Genetics, Population , Genotype , Male
7.
Insect Biochem Mol Biol ; 34(8): 809-22, 2004 Aug.
Article in English | MEDLINE | ID: mdl-15262285

ABSTRACT

The damaging effect of aphids to crops is largely determined by the spectacular rate of increase of populational expansion due to their parthenogenetic generations. Despite this, the molecular processes triggering the transition between the parthenogenetic and sexual phases between their annual life cycle have received little attention. Here, we describe a collection of genes from the cereal aphid Rhopalosiphum padi expressed during the switch from parthenogenetic to sexual reproduction. After cDNA cloning and sequencing, 726 expressed sequence tags (EST) were annotated. The R. padi EST collection contained a substantial number (139) of bacterial endosymbiont sequences. The majority of R. padi cDNAs encoded either unknown proteins (56%) or housekeeping polypeptides (38%). The large proportion of sequences without similarities in the databases is related to both their small size and their high GC content, corresponding probably to the presence of 5'-unstranslated regions. Fifteen genes involved in developmental and differentiation events were identified by similarity to known genes. Some of these may be useful candidates for markers of the early steps of sexual differentiation.


Subject(s)
Aphids/genetics , Aphids/physiology , Expressed Sequence Tags , Gene Expression Regulation, Developmental , Genes, Insect/genetics , Parthenogenesis/genetics , Reproduction/genetics , Amino Acid Sequence , Animals , Base Sequence , Databases, Genetic , Gene Expression Profiling/methods , Gene Library , Molecular Sequence Data
8.
Proc Biol Sci ; 270(1525): 1703-12, 2003 Aug 22.
Article in English | MEDLINE | ID: mdl-12964998

ABSTRACT

In North America, the pea aphid Acyrthosiphon pisum encompasses ecologically and genetically distinct host races that offer an ideal biological system for studies on sympatric speciation. In addition to its obligate symbiont Buchnera, pea aphids harbour several facultative and phylogenetically distant symbionts. We explored the relationships between host races of A. pisum and their symbiotic microbiota to gain insights into the historical process of ecological specialization and symbiotic acquisition in this aphid. We used allozyme and microsatellite markers to analyse the extent of genetic differentiation between populations of A. pisum on pea, alfalfa and clover in France. In parallel, we examined: (i) the distribution of four facultative symbionts; and (ii) the genetic variation in the Buchnera genome across host-associated populations of A. pisum. Our study clearly demonstrates that populations of A. pisum on pea, clover and alfalfa in France are genetically divergent, which indicates that they constitute distinct host races. We also found a very strong association between host races of A. pisum and their symbiotic microbiota. We stress the need for phylogeographic studies to shed light on the process of host-race formation and acquisition of facultative symbionts in A. pisum. We also question the effects of these symbionts on aphid host fitness, including their role in adaptation to a host plant.


Subject(s)
Aphids/genetics , Buchnera/genetics , Gene Frequency/genetics , Microsatellite Repeats/genetics , Phylogeny , Symbiosis/genetics , Adaptation, Biological , Animals , DNA Primers , Ecosystem , Fabaceae , France , Selection, Genetic , Sequence Analysis, DNA
9.
Mol Ecol ; 11(4): 711-23, 2002 Apr.
Article in English | MEDLINE | ID: mdl-11972759

ABSTRACT

Cyclical parthenogens, including aphids, are attractive models for comparing the genetic outcomes of sexual and asexual reproduction, which determine their respective evolutionary advantages. In this study, we examined how reproductive mode shapes genetic structure of sexual (cyclically parthenogenetic) and asexual (obligately parthenogenetic) populations of the aphid Rhopalosiphum padi by comparing microsatellite and allozyme data sets. Allozymes showed little polymorphism, confirming earlier studies with these markers. In contrast, microsatellite loci were highly polymorphic and showed patterns very discordant from allozyme loci. In particular, microsatellites revealed strong heterozygote excess in asexual populations, whereas allozymes showed heterozygote deficits. Various hypotheses are explored that could account for the conflicting results of these two types of genetic markers. A strong differentiation between reproductive modes was found with both types of markers. Microsatellites indicated that sexual populations have high allelic polymorphism and heterozygote deficits (possibly because of population subdivision, inbreeding or selection). Little geographical differentiation was found among sexual populations confirming the large dispersal ability of this aphid. In contrast, asexual populations showed less allelic polymorphism but high heterozygosity at most loci. Two alternative hypotheses are proposed to explain this heterozygosity excess: allele sequence divergence during long-term asexuality or hybrid origin of asexual lineages. Clonal diversity of asexual lineages of R. padi was substantial suggesting that they could have frozen genetic diversity from the pool of sexual lineages. Several widespread asexual genotypes were found to persist through time, as already seen in other aphid species, a feature seemingly consistent with the general-purpose genotype hypothesis.


Subject(s)
Aphids/genetics , Aphids/physiology , Genetics, Population , Reproduction, Asexual/genetics , Reproduction/genetics , Alleles , Animals , Aphids/enzymology , Enzymes/genetics , Female , Gene Frequency , Genetic Variation , Male , Microsatellite Repeats , Parthenogenesis/genetics
10.
Proc Biol Sci ; 268(1483): 2291-9, 2001 Nov 22.
Article in English | MEDLINE | ID: mdl-11703868

ABSTRACT

Cyclical parthenogens, including aphids, are important models for studying the evolution of sex. However, little is known about transitions to asexuality in aphids, although the mode of origin of asexual lineages has important consequences for their level of genetic diversity, ecological adaptability and the outcome of competition with their sexual relatives. Thus, we surveyed nuclear, mitochondrial and biological data obtained on cyclical and obligate parthenogens of the bird cherry-oat aphid, Rhopalosiphum padi (L), to investigate the frequency of transitions from sexuality to permanent asexuality. Many instances of asexual lineages retaining the ability to produce males are known in aphids, so particular attention was paid to the existence of occasional matings between females from sexual lineages and males produced by asexual lineages, which have the potential to produce new asexual lineages. Phylogenetic inference based on microsatellite and mitochondrial data indicates at least three independent origins of asexuality in R. padi, yielding the strongest evidence to date for multiple origins of asexuality in an aphid. Moreover, several lines of evidence demonstrate that transitions to asexuality result from two mechanisms: a complete spontaneous loss of sex and repeated gene flow from essentially asexual lineages into sexual ones.


Subject(s)
Aphids/genetics , Genes, Insect , Parthenogenesis/genetics , Animals , Aphids/classification , DNA, Mitochondrial , Female , Genetic Variation , Haplotypes , Male , Microsatellite Repeats , Reproduction, Asexual/genetics
11.
Biotechniques ; 31(4): 810, 814-6, 818, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11680712

ABSTRACT

By comparing data collected with different automated sequencers and a manual technique (fragment separation in a silver-stained polyacrylamide gel), we found strong discrepancies in allele size of microsatellite loci. To quantify the sizing bias generated by automated capillary electrophoresis, we typed 51 alleles at seven loci andfound that differences between actual (manual) and called (automated) sizing were inversely related to locus size. This result seems independent of the fluorescent dye but might be due to different migration patterns of the size standard and the microsatellite loci. Thus, it is essential to distinguish between actual (that can only be confirmed by sequencing) and called (obtained with automated sequencer) allele sizes. To enable the comparison of data collected by different laboratories on different instruments, the greatest attention should be paid to material and protocol descriptions used for allele sizing, and reference standard DNA genotypes should be shared between collaborating laboratories. Without these precautions, scoring errors in allele size might result in important misleading conclusions.


Subject(s)
Electrophoresis, Capillary/methods , Microsatellite Repeats , Sequence Analysis, DNA/methods , Alleles , Animals , Aphids/genetics , Automation , Biotechnology
12.
Mol Ecol ; 8(6): 965-73, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10434417

ABSTRACT

The aphid Rhopalosiphum padi shows coexistence of sexual and asexual populations, providing an opportunity to study the evolution of breeding system variation in the context of theories on the origin and maintenance of sex. However, assessments of the distribution of sexual and asexual lineages of this aphid are complicated by the difficulties in rapidly characterizing their breeding system. To facilitate this task and to gain insight into the genetic relatedness between sexual and asexual genotypes, molecular markers linked to breeding system differences were recently developed. In this study, we have successfully converted a random amplified polymorphic DNA (RAPD) marker associated with life-cycle variation in R. padi into a codominant sequences-characterized amplified region (SCAR). Segregating and natural populations of known breeding systems were examined to evaluate the life cycle-SCAR marker association. Complete linkage was found in segregating populations while the association averaged 94% in field populations. Detailed analysis of allelic distribution and sequence divergence of the SCAR locus among sexual and asexual populations provides further evidence for a unique and apparently ancient loss of sexuality in this aphid. It also suggests that occasional gene flow occurs between populations differing in their breeding system, mediated by males produced by 'asexual' lineages. This system provides the possibility for the recurrent emergence of new asexual lineages, ensuring the longer persistence of asexuality, and would have important implications for the assessment of costs and benefits of sex in aphids.


Subject(s)
Aphids/genetics , Aphids/physiology , Genetic Markers , Animals , Aphids/growth & development , Base Sequence , Breeding , Cloning, Molecular , DNA, Mitochondrial/chemistry , DNA, Mitochondrial/genetics , Edible Grain , Genetics, Population , Molecular Sequence Data , Parthenogenesis , Random Amplified Polymorphic DNA Technique , Reproduction , Reproduction, Asexual , Restriction Mapping , Sequence Analysis, DNA
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