Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26–q26.1

A large inbred kindred from Pakistan in which an isolated type of split-hand/split-foot anomaly is transmitted as an X-chromosomal trait has previously been described. An X/autosomal translocation and an X-chromosomal rearrangement have been excluded by cytogenetic studies. In order to map the gene responsible for this disorder, linkage analysis has been performed by using 14 highly polymorphic DNA markers distributed over the whole X chromosome. Two-point linkage analysis between the disease locus and X-chromosomal marker loci gives maximal lod scores at = 0.00 with the loci DXS294 (Z _max= 5.13) and HPRT (Z _max= 4.43), respectively, suggesting that the gene for the X-chromosomal split-hand/split-foot anomaly is localized at Xq26–q26.1.     

Aplasia of tibia with split-hand/split-foot deformity. Report of six families with 35 cases and consideration about variability and penetrance

Summary Six families with a total of 34 affected persons with the syndrome of tibial aplasia and ectrodactyly are reported. The spectrum of malformations is compared to that of 99 familial cases from the literature. The full-blown syndrome consists of bilateral aplasia of tibiae and split-hand/split-foot deformity. Additional malformations may be distal hypoplasia or bifurcation of femora, hypo- or aplasia of ulnae, and minor anomalies such as aplasia of patellae, hypoplastic big toes, postaxial and intermediate polydactyly in connection with split-hand deformity, and cup-shaped ears. The mildest visible manifestation may be hypoplastic big toes, the severest is tetramonodactyly or transverse hemimelia. This disorder is autosomal dominantly inherited. The penetrance is markedly reduced.     

Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1

Split-hand/foot malformation with long-bone deficiency (SHFLD) is a rare, severe limb deformity characterized by tibia aplasia with or without split-hand/split-foot deformity. Identification of genetic susceptibility loci for SHFLD has been unsuccessful because of its rare incidence, variable phenotypic expression and associated anomalies, and uncertain inheritance pattern. SHFLD is usually inherited as an autosomal dominant trait with reduced penetrance, although recessive inheritance has also been postulated. We conducted a genomewide linkage analysis, using a 10K SNP array in a large consanguineous family (UR078) from the United Arab Emirates (UAE) who had disease transmission consistent with an autosomal dominant inheritance pattern. The study identified two novel SHFLD susceptibility loci at 1q42.2-q43 (nonparametric linkage [NPL] 9.8, P=.000065) and 6q14.1 (NPL 7.12, P=.000897). These results were also supported by multipoint parametric linkage analysis. Maximum multipoint LOD scores of 3.20 and 3.78 were detected for genomic locations 1q42.2-43 and 6q14.1, respectively, with the use of an autosomal dominant mode of inheritance with reduced penetrance. Haplotype analysis with informative crossovers enabled mapping of the SHFLD loci to a region of approximately 18.38 cM (8.4 Mb) between single-nucleotide polymorphisms rs1124110 and rs535043 on 1q42.2-q43 and to a region of approximately 1.96 cM (4.1 Mb) between rs623155 and rs1547251 on 6q14.1. The study identified two novel loci for the SHFLD phenotype in this UAE family.     

Function of weaponry in females: the use of horns in intrasexual competition for resources in female Soay sheep

In many species, females show reduced expression of a trait that is under sexual selection in males, and this expression is thought to be maintained through genetic associations with the male phenotype. However, there is also the potential for the female trait to convey an advantage in intrasexual conflicts over resources. We tested this hypothesis in a feral population of Soay sheep, in which males and females have a polymorphism for horn development, producing either full (normal horned), reduced (scurred) or no (polled, females only) horns. During the lambing period, females who possessed horns were more likely to initiate and win aggressive interactions, independent of age, weight and birthing status. The occurrence of aggression was also context dependent, decreasing over the lambing period and associated with local density. Our results demonstrate that a trait that confers benefits to males during intrasexual competition for mates may also be used by females in intrasexual competition over resources: males use weaponry to gain mates, whereas females use weaponry to gain food.     

Signal trait sexual dimorphism and mutual sexual selection in Drosophila serrata

Abstract The evolution of sexual dimorphism may occur when natural and sexual selection result in different optimum trait values for males and females. Perhaps the most prominent examples of sexual dimorphism occur in sexually selected traits, for which males usually display exaggerated trait levels, while females may show reduced expression of the trait. In some species, females also exhibit secondary sexual traits that may either be a consequence of a correlated response to sexual selection on males or direct sexual selection for female secondary sexual traits. In this experiment, we simultaneously measure the intersex genetic correlations and the relative strength of sexual selection on males and females for a set of cuticular hydrocarbons in Drosophila serrata . There was significant directional sexual selection on both male and female cuticular hydrocarbons: the strength of sexual selection did not differ among the sexes but males and females preferred different cuticular hydrocarbons. In contrast with many previous studies of sexual dimorphism, intersex genetic correlations were low. The evolution of sexual dimorphism in D. serrata appears to have been achieved by sex-limited expression of traits controlled by genes on the X chromosome and is likely to be in its final stages.     

Female ornamentation and male mate choice in dark-eyed juncos

Traits that enhance attractiveness in one sex may or may not influence attractiveness in the other. In the dark-eyed junco, Junco hyemalis, outer tail feathers of males and females are all or partly white and form a sharp contrast with the bird's mostly grey plumage. The amount of white in these feathers (‘tail white’) is greater in males than in females and, as we report here, is greater in birds that have completed a second prebasic moult than in yearlings. During courtship, male juncos spread their tails, revealing their tail white, and a previous experiment has shown that males with experimentally enhanced tail white are more attractive to females. To determine whether females with experimentally enhanced tail white would be preferred by males, we clipped and replaced tail feathers of females, creating a control group with low to natural levels of tail white and an enhanced group with high levels. We tested preference in a mate choice apparatus like that used previously and found that males courted both control and enhanced females and displayed individual preferences but showed no collective preference for members of either category of females. Because we found neither a preference for trait values that indicate greater age/experience (experimentally enhanced females) nor a preference for less male-like appearance (control females), our results are inconsistent with a role for male mate choice in the maintenance of tail white in females. Female tail white may be subject to selection in another context or persist owing to a genetic correlation between the sexes. Regardless, the sexes apparently prefer different trait values, which suggests that preferences are expressed independently in males and females.     

Genetic analysis of extra sex combs in the hybrids between Drosophila subobscura and D. madeirensis

Drosophila subobscura and D. madeirensis are closely related species, the first distributed over a large area and the latter restricted to the island of Madeira. These species can hybridize in laboratory conditions, yielding fertile females and sterile males. Hybrid offspring show several phenotypic anomalies, including sex combs on the second and third pairs of legs in males. The extra sex comb trait is a homeotic transformation of the mesothoracic and metathoracic legs into prothoracic legs. This anomaly is observed almost exclusively in F₁ males with D. madeirensis mothers. Analysis of backcross males shows that D. subobscura and D. madeirensis have diverged at a minimum of four autosomal loci affecting the extra sex comb anomaly. In addition, some incompatibility involving the X chromosome and/or a maternal effect is also implicated.     

指（趾）骨异常及其相关基因研究进展

指(趾)骨异常是人群中较为常见的一种遗传缺陷,一般为常染色体显性遗传,也有少数以常染色体隐性遗传的方式传递,包括四肢大范围的缺失缺陷,也包括细微的指(趾)数目、长度、解剖形态结构的变化,是由于遗传进化过程中的变异或发育过程中的不良因素(如异常子宫内环境)所致.指(趾)骨异常可以分为多指(趾)并指(趾)症(Synpolydactyly,SPD)、手足裂畸形(split-hand/split-foot malformation,SHFM)和短指(趾)(Brachydactyly,BD).本文综述了指(趾)骨异常的分类及其遗传特点,总结了指(趾)骨异常畸形相关基因的研究进展.     

Male Ornamentation in a Sex‐Role Reversed Pipefish Corythoichthys haematopterus

Sexual selection theory predicts that mating competition in sex‐role reversed animals acts more strongly on females than males and consequently females are expected to develop secondary sexual traits. However, in a sex‐role reversed pipefish Corythoichthys haematopterus (family: Syngnathidae), only males develop an ornamental trait on the thorax, consisting of approx. 3–5 speckles alternated by lateral stripes of brilliant light blue and orange. To understand the function of this male ornament, we examined whether the presence of females affects the expression of this trait, and whether the expression of this trait depends on the male’s physical condition. Individual males were reared in a tank for a month in four different conditions: in high or low food supply and in the presence or absence of a female. After 1 mo, males in better condition expressed larger and deeper blue and yellow speckles, and males maintained with a female expressed larger and deeper blue speckles than solely reared males. These results indicated that the male ornament functions as a signal conveying information on the phenotypic quality of its holder and that females are potential receivers of this signal. Because C. haematopterus exhibits strict monogamy and competition for a mate occurs only among females, we concluded that the male ornament is not displayed in the context of mating competition but rather it is used as a cue for partner recognition to maintain pair bond.     

Autosomal dominant atrial septal defect of ostium secundum type. Report of three families

The authors report on three Sicilian families with 17 individuals (10 females and 7 males) in successive generations affected by atrial septal defect of ostium secundum type (S-ASD) without conduction defect. The anomaly was inherited as an autosomal dominant trait. Cytoplasmic inheritance could be excluded, the anomaly being transmitted also by fathers. Familial S-ASD is probably more frequent than commonly reported since cardiological examination of the relatives is not routinely performed in every case of apparently sporadic ASD.     

Granulomatous skin lesions complicating Varicella infection in a patient with Rothmund-Thomson syndrome and immune deficiency: case report

Acro-cardio-facial syndrome (ACFS) is a rare genetic disorder characterized by split-hand/split-foot malformation (SHFM), facial anomalies, cleft lip/palate, congenital heart defect (CHD), genital anomalies, and mental retardation. Up to now, 9 patients have been described, and most of the reported cases were not surviving the first days or months of age. The spectrum of defects occurring in ACFS is wide, and both interindividual variability and clinical differences among sibs have been reported. The diagnosis is based on clinical criteria, since the genetic mechanism underlying ACFS is still unknown. The differential diagnosis includes other disorders with ectrodactyly, and clefting conditions associated with genital anomalies and heart defects. An autosomal recessive pattern of inheritance has been suggested, based on parental consanguinity and disease's recurrence in sibs in some families. The more appropriate recurrence risk of transmitting the disease for the parents of an affected child seems to be up to one in four. Management of affected patients includes treatment of cardiac, respiratory, and feeding problems by neonatal pediatricians and other specialists. Prognosis of ACFS is poor.     

Correlated changes in male plumage coloration and female mate choice in cardueline finches

The coevolution of extravagant male traits and female mate preferences is a central tenet of sexual selection theory. In lineages in which males have developed more elaborate sexual characters, females favour the most extreme expression of the trait. In some taxa, however, ornamental displays have evolved from more to less exaggerated states. Under these circumstances, it is unclear whether females show preferences for an ancestral male condition or for the current, less elaborate display. Here, we tested female mate preferences relative to male ornamental coloration in two species of cardueline finch (the American goldfinch, Carduelis tristis, and pine siskin, Carduelis pinus) that have evolved less elaborate carotenoid-based colour displays from more elaborately coloured ancestral states. We presented females of each species with a choice of males having either large patches of red colour (the elaborate, ancestral condition) or with species-typical patches of yellow colour (the less elaborate, derived state). Female goldfinches and siskins showed consistent preferences for the natural colour displays of males, and not for the more elaborate, ancestral colour pattern. Previous research on another cardueline finch taxon (a subspecies of the house finch, Carpodacus mexicanus griscomi), however, showed that females prefer more elaborate, ancestral coloration to the current form of reduced colour expression. The lack of congruence between male trait expression and female trait preference in the lineage with the most recently derived reduction in trait expression suggests that there may be evolutionary lags in the correspondence between male traits and female preferences. A shift in the expression of male coloration appears to be the first step towards the evolution of reduced colour displays in these finches.     

Determinisme des anomalies de sex ratio á hérédité paternelle chez le crustacé amphipode Orchestia gammarellus Pallas

Summary

In the amphipod crustacea Orchestia gammarellus (heterogametic species: 2AXY male, 2AXX female), two kinds of sex ratio bias are recorded, hi the first category (thelygeny linked with intersexuality) a parasitic protozoa modifies the sexual phenotype of genetic males and can transform them into intersex males or functional females. This leads to the occurrence of viable 2AYY males and females.

In a second kind of sex ratio bias, males cause hereditary shifts of sex ratio. These ‘paternal sex ratio’ (psr) traits are transmitted by the male at each generation. Psr-f males cause an excess of females, psr-m males an excess of males.

The psr-m trait has a strictly patroclinous mode of transmission, but females from psr-f strains intervene in the expression of psr-f trait. Intra-sib matings are characterized by an excess of males. This characteristic seems to be linked with the age of the female. It disappears during successive brood. A relation between the psr-m and psr-f trait is observed: some psr- m males give psr-f males in the their progeny.

The analysis of crosses between psr-f or psr-m males and YY females allows to discard meiotic drive or sex lethal mortality as causes for the psr traits. Our results are best explained if we suppose that psr-f and psr-m males are XX and that extrachromosomal hereditary factors or transposable genetic elements intervene in the determinism of the psr traits: a psr-m factor able to masculinize all the embryos and a psr-f factor able to masculinize embryos if present in a sufficient amount.     

X-Linked mental retardation with fragile X. a pedigree showing transmission by apparently unaffected males and partial expression in female carriers

Summary A large family is reported in which mental retardation associated with the fragile site at Xq28 was found. Three normal males seemed to have transmitted the trait through their daughters to affected grandchildren.A total of 19 family members were investigated cytogenetically. Mentally retarded males showed macroorchidism and the fragile X. Three mentally retarded females were found, with the fragile X in a high percentage of cells; in contrast, the obligate carriers showed no or only few cells with the fragile X.     

Female preference for trait symmetry in addition to trait size in swordtail fish

Interest in fluctuating asymmetries, random deviations from perfect bilateral symmetry, has spread to studies of sexual selection because of the intriguing idea that females could use the degree of asymmetry of a male trait to assess the genetic quality of potential mates. The evidence that females prefer males with symmetrical sexual signals, however, remains controversial. A problem that applies to most previous studies is that preference for trait size can be misinterpreted as preference for symmetry, even when overall trait size is held constant, if females assess trait size by the largest minimum on one side. If overall trait size is equal between males, the asymmetrical males will have the maximum and minimum trait size, and so preference to mate with symmetrical males could actually reflect a preference to avoid males with the minimum trait on one side. Xiphophorus cortezi females preferred males with symmetrical bar numbers when the minimum number of bars was held constant. The strength of female preference for the symmetrical males was negatively correlated with the strength of preference the same females had for bar number. These results clearly demonstrate that females preferred trait symmetry in addition to trait size.     

Sequential search and the influence of male quality on female mating decisions

 The patterns of phenotypic association between mated males and females depend on the decision rules that individuals employ during search for a mate. We generalize the sequential search rule and examine how the shape of the function that relates a male character to the benefit of a mating decision influences the threshold value of the male trait that induces females to terminate search. If the fitness function is linear the optimal threshold value of a male character increases with the slope of the function. The phenotypic threshold criterion declines, all else being equal, if the fitness function is made more concave (or less convex) by an increase of the risk of the function. The expression of the trait in females has no effect on the optimal threshold value of a male character if the fitness function is linear and phenotypic values combine additively to influence the benefit of a mating decision; the phenotypic threshold criterion is ubiquitous among females. A convex fitness function induces females with high trait values to adopt a relatively high phenotypic threshold criterion, whereas a concave fitness function induces such females to adopt a low threshold value for the male trait. Thus, linear, convex and concave fitness functions effect random, assortative and disassortative combinations of phenotypes among mated individuals, respectively. Changes of female search behavior induced by changes of the distribution of a male character similarly depend on the shape of the fitness function. A variance-preserving increase of male trait values produces a relatively small increase of the threshold criterion for the male character if the fitness function is concave, relative to conditions in which the fitness function is either linear or convex. Our results suggest that a sequential search rule can in principle induce the kinds of mating patterns observed in nature and that the phenotypic association between mated individuals is likely to depend on how a male character translates into fitness, the distribution of the trait among males and attributes of searching females. Received: 20 September 1997 / Revised version: 13 August 1998     

Ectrodactyly/split hand feet malformation

Split-hand/split-foot malformation is a rare limb malformation with median clefts of the hands and feet and aplasia/hypoplasia of the phalanges, metacarpals and metatarsals. When present as an isolated anomaly, it is usually inherited as an autosomal dominant form. We report a case of autosomal recessive inheritance and discuss the antenatal diagnosis, genetic counseling and treatment for the malformation.     

Parasitism and the expression of sexual dimorphism

Although a negative covariance between parasite load and sexually selected trait expression is a requirement of few sexual selection models, such a covariance may be a general result of life‐history allocation trade‐offs. If both allocation to sexually selected traits and to somatic maintenance (immunocompetence) are condition dependent, then in populations where individuals vary in condition, a positive covariance between trait expression and immunocompetence, and thus a negative covariance between trait and parasite load, is expected. We test the prediction that parasite load is generally related to the expression of sexual dimorphism across two breeding seasons in a wild salamander population and show that males have higher trematode parasite loads for their body size than females and that a key sexually selected trait covaries negatively with parasite load in males. We found evidence of a weaker negative relationship between the analogous female trait and parasite infection. These results underscore that parasite infection may covary with expression of sexually selected traits, both within and among species, regardless of the model of sexual selection, and also suggest that the evolution of condition dependence in males may affect the evolution of female trait expression.