Scholarly Literature

This is a database of scholarly literature that concentrates currently on natural and engineered selfish genetic elements (gene drives).  The latest are shown here.
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Behavioral reduction in the transmission of deleterious t-haplotypes by wild house mice

4446
Lenington, SH, I. L.,  The American Naturalist,  137:366-378. 1991-01-04 00:00:00.
About 25% of wild house mice are heterozygous (+/t) for a variable recessive haplotype of the T locus. Although t haplotypes are highly deleterious when homozygous, they are maintained in wild mouse populations because they are associated with transmission-ratio distortion in heterozygous males, which may transmit their t haplotype to 90%-100% of their progeny. In a study of factors affecting variation in male transmission ratio in matings between wild-caught +/t males and +/+ females, we found (1) that male transmission ratio is considerably lower in litters produced as a result of postpartum-estrus matings than in litters produced as a result of cycling-estrus matings, (2) that the frequency of postpartum-estrus litters is much higher when +/t males mate with females caught from the same location as themselves than when they mate with females caught elsewhere, and (3) that, as a result of findings I and 2, the male transmission ratio is considerably lower in within-population matings than in betweenpopulation matings. These data suggest that the frequency of t haplotypes within populations may be correlated with the migration rate and that t haplotypes may be found in high frequencies only in populations for which the migration rate is high.

B-chromosome drive

4445
Jones, RN,  American Naturalist,  137:430-442. 1991-01-03 00:00:00.
The view of B-chromosome polymorphisms that is coming into favor resembles the so-called "parasitic" model, which was first advanced 45 yr ago. Since that time, repeated and ongoing efforts have been made to ascribe an adaptive role to B's (e.g., in terms of phenotypic advantage, effects of variability, etc.), but success in this direction has been singularly lacking. Consistently and repeatedly, the data indicate that harmful effects, or at best neutral or undetectable effects, are associated with B's and provide evidence of the potency of accumulation mechanisms based on drive. Modeling exercises have proved useful in examining these polymorphisms, and of the ones that have been published to date, all have favored drive as the main force generating B-chromosome polymorphisms.

Molecular and chromosomal studies on the origin of t-haplotypes in mice

4444
Hammer, MF,  American Naturalist,  137:359-365. 1991-01-02 00:00:00.
Mouse t haplotypes are variant forms of the proximal third of chromosome 17 that enhance their representation in the gene pool by means of a male-specific transmission-ratio distortion. As with other systems of meiotic drive, they are maintained as independent genetic entities by inversions that suppress recombination with their wild-type homologues. This article reviews some of the evidence for the origin of this complex system based on DNA and chromosomal comparisons. Such comparisons suggest a stepwise evolution of t haplotypes, whereby the proximal and distal inversion occurred on separate chromosomal lineages and at different times. The initial event leading to the spread of t haplotypes may have been an inversion occurring on the wild-type chromosome (nondriving) 2-4 million yr ago. An additional implication of the data is that meiotic drive gives t haplotypes the ability to traverse species boundaries and spread rapidly around the world.

Tsetse fly eradication in Burkina Faso and evaluation of traps and targets

26174
M. Clair, D. Cuisance, H. Politzar, P. Merot and B. Bauer,  STERILE INSECT TECHNIQUE FOR TSETSE CONTROL AND ERADICATION,  1990-05-01 14:50:02.
Control operations against tsetse flies with the sterile insect technique (SIT) were conducted by the Centre de recherches sur les trypanosomoses animales (CRTA) (Institut d’élevage et de médecine vétérinaire des pays tropicaux/Gesellschaft fur Technische Zusammenarbeit (IEMVT/GTZ) Project), Bobo-Dioulasso (Burkina Faso). The project ended in 1984 with the eradication in the Sideradougou pastoral zone ofthe three tsetse species present there (Glossina palpalis gambiensis, G. tachinoides and G. morsitans submorsitans). Since 1985, besides monitoring of this area, the CRTA oriented its activities towards improving trapping by carrying out research on the form and colour of targets as well as the use of olfactory attractants.

Sex-ratio meiotic drive in Drosophila testacea

4462
James, ACJ, J.,  Genetics,  126:651-656. 1990-01-20 00:00:00.
We document the occurrence of "sex ratio" meiotic drive in natural populations of Drosophila testacea. "Sex ratio" males sire greater than 95% female offspring. Genetic analysis reveals that this effect is due to a meiotically driven X chromosome, as in other species of Drosophila in which "sex ratio" has been found. In contrast to other drosophilids, the "sex ratio" and standard chromosomes of D. testacea do not differ in gene arrangement, implying that the effect may be due to a single genetic factor in this species. In all likelihood, the "sex ratio" condition has evolved independently in D. testacea and in the Drosophila obscura species group, as the loci responsible for the effect occur on different chromosomal elements. An important ecological consequence of "sex ratio" is that natural populations of D. testacea exhibit a strong female bias. Because D. testacea mates, oviposits, and feeds as adults and larvae on mushrooms, this species provides an excellent opportunity to study the selective factors in nature that prevent "sex ratio" chromosomes from increasing to fixation and causing the extinction of the species.

Evolution of the segregation ratio – Modification of gene conversion and meiotic drive

4461
Bengtsson, BOU, M. K.,  Theoretical Population Biology,  38:192-218. 1990-01-19 00:00:00.
We compare the evolutionary pressures that direct the modification of gene conversion and meiotic drive at loci subject to purifying and overdominant viability selection. Gene conversion differs from meiotic drive in that modifers do not affect their own segregation ratios, even when linked to the viability locus. Segregation distortion generates gametic level disequilibria between alleles at the viability locus and modifiers of gene conversion and meiotic drive: enhancers of segregation distortion become positively associated with driven alleles. Suppression of gene conversion evolves if the driven allele is marginally disadvantageous (overdominant viability selection), and higher rates evolve if the driven alleles are relatively advantageous (purifying viability selection). Gametic disequilibria permit enhancers of meiotic drive that are linked to the driven locus to promote their own segregation. We attribute the failure of genetic modifiers of gene conversion and meiotic drive to maximinize mean fitness to the generation of such associations.

Meiotic drive in female mice heterozygous for the HSR inserts on Chromosome-1

4460
Agulnik, SIA, A. I.; Ruvinsky, A. O.,  Genetical Research,  55:97-100. 1990-01-18 00:00:00.
Chromosome 1 with one or two long insertions has been previously found in natural mouse populations. The inheritance of chromosome 1 with two insertions from the Yakutsk population is analysed in this paper. It was demonstrated that heterozygous females transmit this chromosome to 80–85% of offspring. The observations made at M II, in conjunction with the recombination data, allowed us to conclude that preferential passage of the chromosome 1 with insertions to the oocyte and egg, rather than to the first and second polar bodies at meiosis, is the causative factor of the distorted segregation. A meiotic drive of such potency has not been previously reported for female mammals. The possible mechanism of the drive is discussed.

Meiotic drive of the aberrant Chromosome-1 in the house mouse

4459
Agulnik, SIA, A. I.; Ruvinsky, A. O.,  Genetika,  26:664-669. 1990-01-17 00:00:00.
Animals with aberrant chromosome 1 carrying one or two large insertions were earlier described in natural populations of Mus musculus. In the present work, inheritance of the aberrant chromosome 1 from the Yakutsk population was investigated. It was shown that 80-85% of the progeny from heterozygous females received chromosome 1 with insertions. From chromosomal analysis of blastocytes and oocytes at the MII stage, it was concluded that the preferential distribution of the aberrant chromosome into oocytes during the first and especially, the second meiotic divisions is relevant to the segregation distortion observed. The mechanism of this powerful meiotic drive is discussed.

Rapid spread of transposable P elements in experimental populations of Drosophila melanogaster.

6265
A. G. Good, G. A. Meister, H. W. Brock, T. A. Grigliatti and D. A. Hickey,  Genetics,  1223:387-396. 1989-05-08 16:20:58.
The invasion of P elements in natural populations of Drosophila melanogaster was modeled by establishing laboratory populations with 1 %, 5% and 10% P genomes and monitoring the populations for 20 generations. In one experiment, the ability of flies to either induce or suppress gonadal sterility in different generations was correlated with the amount of P element DNA. In a second experiment, the percentage of genomes that contained P elements, and the distribution of P elements among individual flies was monitored. The ability to induce gonadal dysgenesis increased rapidly each generation. However, the increase in P cytotype lagged behind by five to ten generations. The total amount of P element DNA and the frequency of flies containing P elements increased each generation. The number of P elements within individual genomes decreased initially, but then increased. Finally, the distribution of P elements within the genomes of individuals from later generations varied considerably, and this pattern differed from the parental P strain. These results suggest that the interaction between the assortment and recombination of chromosomal segments, and multiplicative transposition could result in the rapid spread of P elements in natural populations

Genetics-driving genes and chromosomes

4463
Charlesworth, B,  Nature,  332:394-395. 1988-01-21 00:00:00.
Thereare several genetic and chromosomal systems in which Mendel's first law - the equal probability of transmission of maternal and paternal alternative alleles or homologues - is violated. This phenomenon was named 'meiotic drive' in 1957 by Sandler and Novitski, who drew attention to the fact that it operates as an evolutionary force which can cause an increase in the population frequency of the allele or chromosome which is favoured in transmission, even if it confers a disadvantage on its carriers in terms of fitness at the level of the individual

Methods for replacement of malaria vector populations

4464
Curtis, CFG, P. M.,  American Journal of Tropical Medicine and Hygiene,  91:43-48. 1988-01-02 00:00:00.
The prospects are reviewed of replacement of malaria vector populations by harmless mosquito populations by means of: (i) ecologically competitive non-vector species; (ii) natural selection due to the harmfulness of being infected; (iii) selection for insecticide resistance genes; (iv) meiotic drive; (v) negative heterosis; and (vi) hybrid dysgenesis. Serious difficulties exist with all of these approaches. At present 'dilution', i.e. release of insects carrying the desired genes without any system for forcing population replacement is the only available method. It avoids the disadvantage that, in constructing elaborate genetic 'packages', factors for low fitness may be irreversibly incorporated into them. It is debatable whether release of males only or both sexes should be attempted.

Thte genetic basis of resistance and sensitivity to the meiotic drive gene D in the mosquito Aedes aegypti L.

4469
Wood, RJO, N. A.,  Genetica,  72:69-79. 1987-01-07 00:00:00.
A study has been made on the genetic basis of meiotic drive at the Distorter (D) locus which, in coupling with the male-determining gene (or region) M on the Y chromosome, causes production of excess male progeny. Its effect is regulated by the sensitivity/resistance of the X chromosome. This study demonstrates that there are two major loci controlling resistance/sensitivity to MD: (1) the m gene (or region) on the X chromosome (allelic with M) which may be either m R or m S (resistant or sensitive), (2) the t (tolerance) gene (or genes) which recombines with m and, if present, largely counteracts the effect of m S . There is also evidence that MD itself is capable of limited adaptation.; ; The conclusions were derived from using MD males of the T30 or ACCRA strains (from Trinidad and Ghana respectively). The work involved the use of the CHIPEI and RED strains with sensitive X chromosomes, the latter also carrying the t (tolerance) gene which is linked to re (red eye) and m (the sex-determining locus or region) but recombines with both. The implications of these findings for using MD as a method of population control are discussed.

Abnormal salivary gland puff associated with meiotic drive in mosquitos (Diptera, Culicidae)

4468
Sweeny, TLG, P.; Barr, A. R.,  Journal of Medical Entomology,  24:623-627. 1987-01-06 00:00:00.
A meiotic drive factor, distorter (d), has been described previously for Culex pipiens L. mosquitoes. Males homozygous for the gene (Md/md) produce few female offspring owing to breakage of the female-determining dyad of chromosome 1 (the sex chromosome) during the first meiotic division of spermatogenesis. Orcein squash preparations of polytene salivary gland chromosomes of the distorter strain revealed a chromosome break and other abnormalities at zone 10C3, the location of a large puff that has been reported to be associated with sex determination in C. pipiens. In the polytene chromosomes, d apparently disrupts normal expansion and contraction of the puff. Zone 10C3 probably is also the breakpoint of the female-determining dyad. Zone 10C3 on the male-determining dyad seems to be resistant to the action of d, whereas zone 10C3 on the female-determining dyad is vulnerable to the destructive action of d. Possibly the break in the female-determining dyad occurs directly at m, the gene locus for "femaleness" in C. pipiens, in which case d may be a mutated form of m.

Control of meiotic drive of B-chromosomes in the mealybug, Pseudococcus affinis (obscurus)

4467
Nur, UB, B. L. H.,  Genetics,  115:499-510. 1987-01-05 00:00:00.
Isofemale lines of Pseudococcus affznis (MASKELL) differ in their ability to maintain B chromosomes (Bs) due to the presence of genotypes that affect the rate of transmission (k) of the Bs. The nature of these genotypes was analyzed by comparing ks of males carrying the same B and the same paternal genome (which is heterochromatic), but differing in their maternal genome. In males from line L-60, which maintained the B at a frequency of over 4.0 Bs per individual, the mean k varied between 0.7 and 0.95 in different experiments. Over the same period, the mean k of males with a maternal genome from one of two lines in which the B was rapidly lost (L-1 19), increased from 0.5 to 0.9, and that of the other line (L-230) decreased gradually from 0.6 to less than 0.1. The ks appear not to be correlated with the geographical or parental origin of the B. The observed changes in k are attributed at least in part to changes in the frequency of genotypes (alleles) which can drastically reduce the transmission of the B and, when present in high frequency, can lead to its rapid loss. The frequency distribution of the ks of sons of F, females from the cross L-230 X L-60 suggests that the two lines differ at two unlinked loci with additive effects on k. The genome of L-119 also caused the B to undergo nondisjunction in about 10% of the primary spermatocytes. A comparison between the ks of the males tested and those of males from a natural population suggests that in that population the B is “parasitic” and that the frequency of transmission-reducing genotypes is low.

X-4 Translocation and meiotic drive in Drosophila melanogaster males: Role of sex chromosome pairing

4466
McKee, B,  Genetics,  116:409-413. 1987-01-04 00:00:00.
Males carrying certain X-4 translocations exhibit strongly skewed sperm recovery ratios. The Xp4D half of the translocation disjoins regularly from the Y chromosome and the 4‘XD half disjoins regularly from the normal 4. Yet the smaller member of each bivalent is recovered in excess of its pairing partner, apparently due to differential gametic lethality. Chromosome recovery probabilities are multiplicative; the viability of each genotype is the product of the recovery probability of its component chromosomes. Meiotic drive can also be caused by deficiency for X heterochromatin. In( I)scQLscBR males show the same size dependent chromosome recoveries and multiplicative recovery probabilities found in T(1;4)Bs males. Meiotic drive in Zn(I)scQLscBR males has been shown to be due to X-Y pairing failure. Although pairing is regular in the T(X;4) males, the striking phenotypic parallels suggest a common explanation. The experiments described below show that the two phenomena are, in fact, one and the same. X-4 translocations are shown to have the same effect on recovery of independently assorting chromosomes as does Zn(I)scqLscgR. Addition of pairing sites to the 4pXD half of the translocation eliminates drive. A common explanation-failure of the distal euchromatic portion of the X chromosome to participate in XY meiotic pairing-is suggested as the cause for drive. The effect of X chromosome breakpoint on X-4 translocation induced meiotic drive is investigated. It is found that translocations with breakpoints distal to 13C on the salivary map do not cause drive while translocations broken proximal to 13C cause drive. The level of drive is related to the position of the breakpoint-the more proximal the breakpoint the greater the drive.

Meiotic drive in the sex-chromosome system of the varying lemming, Dicrostonyx torquatus Pall (Rodentia, Microtinae)

4465
Gileva, EA,  Heredity,  59:383-389. 1987-01-03 00:00:00.
In the varying lemming, numerous fertile XY females occur regularly due to the X-linked mutation (X*). Their frequency both in natural populations and laboratory colonies turned out to be about twice higher than that expected under random segregation of heterochromosomes in both sexes. It has been shown in experiments that an excess of XY females resulted from a preferential segregation of the Y chromosome in males. Segregation distortion is not produced by selective embryonal mortality. Meiotic drive of the Y chromosome also causes a significant decrease of sex ratio. Although in the varying lemming meiotic drive is rather weak (the segregation ratio of the Y being 0·54–0·59), it seems to contribute essentially to the evolutionary spread and the maintenance of the X* mutation in populations. The example of Dicrostonyx and probably of other microtines also demonstrates the possible role of meiotic drive in the regulation of the population sex ratio in mammals.

The eradication of Glossina-palpalis-palpalis (Robineau-Desvoidy) (diptera, Glossinidae) using traps, insecticide-impregnated targets and the sterile insect technique in central Nigeria

26155
W. Takken, M. A. Oladunmade, L. Dengwat, H. U. Feldmann, J. A. Onah, S. O. Tenabe and H. J. Hamann,  Bulletin of Entomological Research,  76:275-286. 1986-06-01 13:33:24.
The integrated use of biconical traps, insecticide-impregnated targets and the sterile insect technique was developed for the eradication of Glossina palpalis palpalis (Robineau-Desvoidy) in a 1500-km2 area of central Nigeria. Six weeks or more of continuous removal trapping, using biconical traps, reduced the target tsetse population by more than 90% but failed to eradicate it. Males sterilized by irradiation from a ^Co source that were then released weekly induced significant sterility in target females and were successful in helping to eradicate the target population. A minimum ratio of 10:1 of sterile to wild males was required to achieve eradication in a central area of 300 km2. In marginal habitats, insecticide-impregnated targets were found adequate to control the tsetse population. The targets were also efficient as barriers to prevent reinvasion of the area. The combined effect of removal trapping and sterile male release is expected to eradicate G. p. palpalis from the entire study area.

Detection of Rsp and modifier variation in the meiotic drive system Segregation Distorter (SD) of Drosophila melanogaster

4470
Lyttle, TWB, J. G.; Ganetzky, B.,  Genetics,  114:183-202. 1986-01-08 00:00:00.
Identification of allelic variability at the two major loci (Sd and Rsp) that interact to cause sperm dysfunction in Segregation distorter (SD) males of D. melanogaster has been hampered by the difficulty in separating the elements recombinationally. In addition, small differences in the strength of Sd alleles or sensitivities of Rsp alleles to Sd are difficult to measure against background genetic or environmental variation. Viability effects of the markers used to score progeny classes may also introduce a bias. Removal of Sd and E(SD) from their second chromosome location to create a Dp(2;Y)Sd E(SD) chromosome eliminates these problems, since any combination of Rsp alleles can be easily tested without resorting to recombinational techniques. Further, since these pairs of Rsp alleles are compared in their response to Dp Sd E(SD) in the same individual males, background variation and viability effects can be easily removed to allow finescale resolution of Rsp differences. Tests of all possible pairwise combination of six laboratory chromosomes in this way revealed at least three and possibly four different Rsp allelic classes. In addition, the hierarchical nature of the tests further allowed for determination of the presence of linked suppressors or enhancers of Sd activity. A sample of 11 second chromosomes selected from a group recently isolated from a natural population was also unambiguously ordered as to Rsp allelic status using this approach. The resultant pattern was similar to that obtained for the laboratory chromosomes, except for the not unexpected observation that the natural population apparently harbored more drive suppressors. The pattern of results obtained from these pairwise combinations of Rsp alleles supports the notion that there are no dominance interactions within the group, but that each responds more or less independently to Sd in giving sperm dysfunction.

Tthe genetic control of meiotic drive acting on the B-chromosome of Myrmeleotettix maculatus (Orthoptera, Aacrididae)

4473
Shaw, MWH, G. M.,  Heredity,  54:187-194. 1985-01-11 00:00:00.
Crosses between populations with and without B-chromosomes were made, and backcrossed to the non B parent for two generations. No polygenic differences in male or female meiotic transmission were found, but a modifier of meiotic drive segregated in the experiment, drastically reducing female transmission rate. We tentatively interpret this as evidence of a coevolutionary race between the B-chromosome and the A genome.

Polymorphism in the rates of meiotic drive acting on the B-chromosome of Myrmeleotettix maculatus

4472
Shaw, MWH, G. M.; Anderson, D. A.,  Heredity,  55:61-68. 1985-01-10 00:00:00.
A survey of all the available data on meiotic transmission rates in M. maculatus suggests that a polymorphism in female transmission rate exists in most natural populations. Differences in the frequency of the types or in the transmission rates they manifest may exist between populations or over time, but the evidence is not compelling. The data on males are also equivocal, especially because the environment may affect male transmission rate. We suggest that the polymorphism in female rates may demonstrate the selective equilibrium between the B and the genome in which it exists.

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