Ancestral state reconstruction analysis of hymenopteran sex determination mechanisms

We provide the first phylogenetic evidence supporting complementary sex determination (CSD) as the ancestral mechanism for haplodiploidy in the Hymenoptera. It is currently not possible, however, to distinguish the evolutionary polarity of single locus (sl) CSD and multiple‐locus (ml) CSD given the available data. In this light, we discuss the seemingly maladaptive hypothesis of ml‐CSD ancestry, suggesting that collapse from ml‐CSD to sl‐CSD should remain a viable evolutionary hypothesis based on (i) likely weakening of frequency‐dependent selection on sex alleles under ml‐CSD and (ii) recent findings with respect to the evolutionary novelty of the complementary sex determiner gene in honeybees. Our findings help provide a phylogenetically informed blueprint for future sampling of sex determination mechanisms in the Hymenoptera, as they yield hypotheses for many unsampled or ambiguous taxa and highlight taxa whose further sampling will influence reconstruction of the evolutionary polarity of sex determination mechanisms in major clades.     

膜翅目昆虫的性别决定机制

昆虫性别决定机制存在多样性和复杂性,其中膜翅目昆虫的性别决定由单双倍体决定,单倍体为雄性,二倍体为雌性。本文就膜翅目昆虫的性别决定模式和分子机制进行综述。膜翅目昆虫性别决定有6种模式,即互补性性别决定(complementary sex determination, CSD)、多位点互补性性别决定(multiple-locus CSD, ml-CSD)、基因组印记、母体效应、内共生体诱导产雌单性生殖、父本遗传基因组消除(paternal genome elimination, PGE)。其中,CSD机制是目前在膜翅目昆虫中普遍接受的性别决定模式。而蜜蜂的CSD性别决定机制是膜翅目昆虫性别决定模式中的典型代表,受csd→fem→dsx这一调控级联的控制。     

A Test of the Mating Limitation Hypothesis for Caste Determination in Evylaeus albipes (Hymenoptera: Halictidae), a Primitively Eusocial Halictine Bee

Yanega's (1997) mating limitation hypothesis (MLH) states that if a female mates promptly after emerging, she then becomes a member of the maximally reproductive behavioral caste (i.e., in most cases an overwintering gyne). Females that do not mate early become workers. We tested the MLH in laboratory colonies of a eusocial population of Evylaeus albipes. Of 24 worker brood females (13 from queenright and 11 from orphaned nests), 13 mated on the first day of flight activity and all mated within the first 5 days; there were no significant differences between mating rates of females from the two colony types. All 24 commenced foraging as workers after an average of between 3 and 4 days postmating. We conclude that the MLH does not apply to this species despite the fact that the only known halictine for which this hypothesis has been experimentally tested is the fairly closely related E. marginatus.     

Evolutionary stability of sex chromosomes in snakes

Amniote vertebrates possess various mechanisms of sex determination, but their variability is not equally distributed. The large evolutionary stability of sex chromosomes in viviparous mammals and birds was believed to be connected with their endothermy. However, some ectotherm lineages seem to be comparably conserved in sex determination, but previously there was a lack of molecular evidence to confirm this. Here, we document a stability of sex chromosomes in advanced snakes based on the testing of Z-specificity of genes using quantitative PCR (qPCR) across 37 snake species (our qPCR technique is suitable for molecular sexing in potentially all advanced snakes). We discovered that at least part of sex chromosomes is homologous across all families of caenophidian snakes (Acrochordidae, Xenodermatidae, Pareatidae, Viperidae, Homalopsidae, Colubridae, Elapidae and Lamprophiidae). The emergence of differentiated sex chromosomes can be dated back to about 60 Ma and preceded the extensive diversification of advanced snakes, the group with more than 3000 species. The Z-specific genes of caenophidian snakes are (pseudo)autosomal in the members of the snake families Pythonidae, Xenopeltidae, Boidae, Erycidae and Sanziniidae, as well as in outgroups with differentiated sex chromosomes such as monitor lizards, iguanas and chameleons. Along with iguanas, advanced snakes are therefore another example of ectothermic amniotes with a long-term stability of sex chromosomes comparable with endotherms.     

膜翅目昆虫补偿性性别决定机制

膜翅目昆虫单双倍体性别决定机制(雄性是单倍体、雌性是二倍体)在昆虫纲的进化中有非常重要的作用。通常膜翅目昆虫的性别由单一位点的等位基因决定,杂合体发育成雌性,半合体发育成雄性。在近亲繁殖的情况下,一定数目的雄性会出现纯合二倍体,由于遗传阻隔这种二倍体的雄性通常是不育的。csd基因的发现为膜翅目昆虫性别决定机制提供了分子生物学证据。文章探讨CSD的分子生物学基础,对膜翅目昆虫sl-CSD的分布进行综述并且探讨膜翅目昆虫降低二倍体雄性消耗的策略以及可能存在的进化机制,最后提出几点建议以便从遗传学、生态学以及进化生物学角度全面的了解sl-CSD。     

Effects of a juvenile hormone analogue on honey bee foraging behaviour and alarm pheromone production

Worker honey bees treated with 250 μg of the juvenile hormone analogue methoprene shifted from the broodnest to the food storage region prematurely and displayed precocious foraging behaviour. Treatments with 25 and 2.5 μg caused slight but non-significant effects. Methoprene did not influence individual foraging performance as measured by mean number of foraging trips/h, mean amount of time spent foraging/h or mean duration of the total foraging period. Methoprene also induced premature production of two alarm pheromones, 2-heptanone and isopentyl acetate. These results support the hypothesis that juvenile hormone regulates temporal division of labour in the honey bee colony.     

Demand for Task Performance and Workforce Replacement: Undertakers in Honeybee, Apis mellifera, Colonies

Undertakers are a specialized task group of honey bees that remove dead bees from the colony. The mean adult age of undertakers is 12.5 days; this is similar to that of other specialized task groups, such as guards. The mean number of undertakers in colonies was 544. However, because the number of bees expressing this behavior is dependent on the demand for task performance, undertaker estimates vary depending on the experimental technique. Increasing the demand for undertaking resulted in more bees engaging in the task. Depleting the number of undertakers by removal of bees carrying corpses resulted in new bees assuming undertaking duties. These results support a response-threshold model for engagement of worker bees in task performance.     

Microsatellite DNA analysis reveals low diploid male production in a communal bee with inbreeding

The mechanism of sex determination assumed widespread in parthenogenetically arrhen-otokous Hymenoptera is that of single locus complementary sex determination (CSD). Functionally sterile diploid males are produced under CSD and generate a genetic load, the cost of which increases with inbreeding. We quantify diploid male production (DMP, proportion of diploid individuals that are male) using a morphological criterion (adult fresh weight) and genetical (microsatellite DNA) markers in a communal, sexually size-dimorphic bee, Andrma scotica , which inbreeds. Male genotypes suggested a DMP of 0.003. The inbreeding coefficient, f , was significandy positive (+ 0.165), equivalent to 44% of matings being among full sibs (predicted DMP of 0.11). We hypothesize three non-mutually exclusive explanations to account for the large difference between the low observed (in males) and high expected (derived fromy f for females) DMP: (i) multilocus CSD, (ii) 'sex allele signalling' tied to mate selection, and (iii) sperm selection within mated females. The costs of inbreeding through DMP are apparendy low in A. scotica .     

SEX RATIO SELECTION AND THE EVOLUTION OF ENVIRONMENTAL SEX DETERMINATION IN LABORATORY POPULATIONS OF MENIDIA MENIDIA

What happens when a population with environmental sex determination (ESD) experiences a change to an extreme environment that causes a highly unbalanced sex ratio? Theory predicts that frequency-dependent selection would increase the proportion of the minority sex and decrease the level of ESD in subsequent generations. We empirically modeled this process by maintaining five laboratory populations of a fish with temperature-dependent sex determination (the Atlantic silverside, Menidia menidia) in extreme constant temperature environments that caused highly skewed sex ratios to occur initially. Increases in the minority sex consistently occurred from one generation to the next across all five populations, first establishing and then maintaining a balanced sex ratio until termination of the experiment at 8 to 10 generations. The extent to which the level of ESD changed as balanced sex ratios evolved, however, was not consistent. Two populations that experienced high temperatures each generation displayed a loss of ESD, and in one of these ESD was virtually eliminated. This suggests that temperature-insensitive, sex-determining genes were being selected. In populations maintained in low temperature environments, however, the level of ESD did not decline. Instead, the response of sex ratio to temperature was adjusted upward or downward, perhaps by selection of sex-determining genes sensitive to higher (or lower) temperatures. The two different outcomes at low versus high temperatures occurred independent of the geographic origin of the founding population. Our results demonstrate that ESD is capable of evolving in response to selection.