The genetics of the mimetic butterfly Papilio memnon L

Papilio memnon is a swallowtail butterfly widely distributed in south-east Asia. The females are highly polymorphic and many of them are mimetic. The mode of inheritance of seventeen of the female forms is reported. In contradistinction to earlier work it has been shown that they are controlled by what appears to be a series of at least eleven autosomal alleles at one locus, sexcontrolled to the female in effect. There is evidence, however, that the locus is complex, comprising at least three closely linked loci with occasional occurrence of crossing over between them. Two characters which are not polymorphic and one which may be polymorphic are controlled by genes unlinked to the complex locus (the super-gene). In general, dominance is complete between sympatric forms but absent when they are allopatric. The resemblance between the mimetic forms of P. memnon and their models is greater in the genecomplex of a race in which the allelomorph occurs than in hybrids with a race in which it does not. Thus in no case is the resemblance better in the race cross, in ten cases there is no change and in thirty-five the mimicry is less good. The genetic control of the polymorphism in P. memnon shows remarkable parallels with that in P. dardanus and provides further supporting evidence for Fisher’s and Ford’s view that mimicry evolved gradually by adjustment of the gene-complex as a result of natural selection favouring those wing patterns which most closely resembled the models. Furthermore, as in P. dardanus, the mimicry is controlled by what appears to be a super-gene, adding weight to the conclusion that the genetic control of the polymorphic Batesian mimicry has evolved gradually by the accumulation of closely linked allelomorphs in advantageous combinations. This contrasts with the genetic control of Mullerian mimicry as evidenced in the Heliconids. In P. memnon the dominance relationships of the monomorphic tailed and tailless condition (excluding the form achates ) indicate that dominance can be evolved even when the characters concerned are not polymorphic. In addition, the lower frequency of dominance between allopatric forms than between sympatric ones is strongly in favour of the view that dominance has evolved. Similar evidence has been found from breeding work in the Heliconids and in P. dardanus ; however, the phenomenon is not confined to mimetic situations since there is also evidence for the evolution of dominance in other polymorphisms including industrial melanism.

Genetics ◽  
2002 ◽  
Vol 162 (1) ◽  
pp. 381-394 ◽  
Author(s):  
Craig A Webb ◽  
Todd E Richter ◽  
Nicholas C Collins ◽  
Marie Nicolas ◽  
Harold N Trick ◽  
...  

AbstractIn maize, the Rp3 gene confers resistance to common rust caused by Puccinia sorghi. Flanking marker analysis of rust-susceptible rp3 variants suggested that most of them arose via unequal crossing over, indicating that rp3 is a complex locus like rp1. The PIC13 probe identifies a nucleotide binding site-leucine-rich repeat (NBS-LRR) gene family that maps to the complex. Rp3 variants show losses of PIC13 family members relative to the resistant parents when probed with PIC13, indicating that the Rp3 gene is a member of this family. Gel blots and sequence analysis suggest that at least 9 family members are at the locus in most Rp3-carrying lines and that at least 5 of these are transcribed in the Rp3-A haplotype. The coding regions of 14 family members, isolated from three different Rp3-carrying haplotypes, had DNA sequence identities from 93 to 99%. Partial sequencing of clones of a BAC contig spanning the rp3 locus in the maize inbred line B73 identified five different PIC13 paralogues in a region of ∼140 kb.


1974 ◽  
Vol 16 (4) ◽  
pp. 857-860 ◽  
Author(s):  
K. M. S. Saxena ◽  
A. L. Hooker

In maize (Zea mays L.) Rp3 expresses itself as a dominant gene for resistance to Puccinia sorghi Schw. culture 90laba and as a recessive gene for resistance to culture 933a. Suspecting that Rp3 is a complex locus consisting of two closely linked genes, efforts were made to separate the two putative genes by crossing over. Maize lines heterozygous for resistance and glossy leaf genes (Rp3 - Gl6/rp3 - gl6) were crossed with inbreds homozygous for susceptibility and glossy leaves (rp3 - gl6/rp3 - gl6). The testcross progeny, consisting of 4802 seedlings, was tested with culture 90laba. Fifty-seven recombinant seedlings, resistant to culture 90laba and glossy, were isolated and grown to maturity. These were selfed and their progeny tested to identify those that may have arisen from crossing over within region Rp3. No recombinants of this nature were found. If Rp3 is a complex locus, the two genes comprising it could not be more than 0.06 map units apart.


Genetics ◽  
1978 ◽  
Vol 90 (1) ◽  
pp. 133-149
Author(s):  
Margaret Y Menzel ◽  
Meta S Brown ◽  
Safia Naqi

ABSTRACT The genus Gossypium is favorable for study of genome divergence at several levels. Early stages of divergence have been studied among four D genomes by comparing chiasma frequencies (reciprocal exchanges) between pairs of genomes and between individual counterpart chromosomes marked by heterozygous translocations. D5 (G. raimondii) shows barely detectable differentiation from from Dh (G. hirsutum), whereas D7 (G. lobatum) is considerably less closely related to Dh than is D5. Fragmentary data suggest that D2-2 (G. harknessii) falls between D5 and D7 in its relationship to Dh. Since chiasma frequencies in individual chromosomes and marked regions exhibit the same order of relationships as their corresponding whole genomes, it is concluded that the genome differentiation is generalized (i.e., nucleus-wide) rather than localized in specific chromosomes or chromosome regions. Estimates of relationships based on reciprocal exchange frequencies agree with those based upon preferential synapsis in allohexaploids reported previously. Since preferential synapsis and reciprocal exchange frequencies reveal the same order of relationships, it is concluded that to some extent they reflect common underlying changes in chromosome properties, despite recent evidence that synapsis and crossing over are under independent genetic control.


Nature ◽  
1959 ◽  
Vol 183 (4666) ◽  
pp. 918-921 ◽  
Author(s):  
H. B. D. KETTLEWELL

1970 ◽  
Vol 12 (3) ◽  
pp. 635-650 ◽  
Author(s):  
Satish C. Bhalla

Two sex linked paracentric inversions one on m chromosome, marked with bz (bronze body) and the other on M chromosome, marked with w (white eye), were artificially induced with X-irradiation and isolated. The inversions are designated as In. (1)1 and In. (1)2 respectively. The former is more than 23 units long and the later more than 16 units. Both suppress crossing over markedly and are associated with partial sterility. The two inversions are utilized as crossover suppressors in a technique designed for detecting sex linked recessive lethals. The technique works satisfactorily with certain limitations. The possibility of combining inversions with other chromosomal aberrations for genetic control of Aedes aegypti populations is suggested.


Genetics ◽  
1960 ◽  
Vol 45 (3) ◽  
pp. 345-357
Author(s):  
Ellen C Weaver

1981 ◽  
Vol 1 (10) ◽  
pp. 891-901
Author(s):  
R E Malone ◽  
R E Esposito

We have utilized the single equational meiotic division conferred by the spo13-1 mutation of Saccharomyces cerevisiae (S. Klapholtz and R. E. Esposito, Genetics 96:589-611, 1980) as a technique to study the genetic control of meiotic recombination and to analyze the meiotic effects of several radiation-sensitive mutations (rad6-1, rad50-1, and rad52-1) which have been reported to reduce meiotic recombination (Game et al., Genetics 94:51-68, 1980); Prakash et al., Genetics 94:31-50, 1980). The spo13-1 mutation eliminates the meiosis I reductional segregation, but does not significantly affect other meiotic events (including recombination). Because of the unique meiosis it confers, the spo13-1 mutation provides an opportunity to recover viable meiotic products in a Rec- background. In contrast to the single rad50-1 mutant, we found that the double rad50-1 spo13-1 mutant produced viable ascospores after meiosis and sporulation. These spores were nonrecombinant: meiotic crossing-over was reduced at least 150-fold, and no increase in meiotic gene conversion was observed over mitotic background levels. The rad50-1 mutation did not, however, confer a Rec- phenotype in mitosis; rather, it increased both spontaneous crossing-over and gene conversion. The spore inviability conferred by the single rad6-1 and rad52-1 mutations was not eliminated by the presence of the spo13-1 mutation. Thus, only the rad50 gene has been unambiguously identified by analysis of viable meiotic ascospores as a component of the meiotic recombination system.


1973 ◽  
Vol 22 (1) ◽  
pp. 101-111 ◽  
Author(s):  
Judith Stamberg ◽  
Y. Koltin

SUMMARYTwo strains ofS. communecharacterized by different levels of high recombination frequency in a particular region of the genome (between the two subunits, α and β, of theBincompatibility factor) were crossed, and their progeny tested for recombination frequency in the same region. The difference between the strains in recombination frequency is found to be due to some factor located within the recombining region itself.The segregation among the progeny indicates that the factor consists of a number of sites, with additive effects. This and the dominance relationships suggest that these sites may be recognition sites which comprise a part of the fine control of recombination.


Commonly accepted precepts are challenged : (1) that homologous chromosome pairing is normally mediated by nuclear envelope attachment sites; (2) that crossover site establishment awaits synaptic completion; and (3) that it is the function of the synaptonemal complex to hold homologues in register so that equal crossing over can occur, and perhaps to provide machinery for the crossover process. Although these views may eventually be shown to be true, it is felt that currently available evidence does not warrant their full acceptance, and that alternatives should be considered. As examples of alternatives the following ideas, with some supporting evidence, are suggested: (1) homologous chromsome pairing (in non-haplont organisms) may be accomplished by chance meeting of homologue segments (followed by establishment of invisible, elastic connectors) at congression for a mitotic metaphase (in many cases perhaps the premeiotic mitosis); (2) crossover sites may be established before, during, or immediately following initiation of synapsis; and (3) the synaptonemal complex may somehow function in the crossover process at the inception of its formation, but its complete deployment throughout each normal bivalent may serve some other role, such as mediation of the binding of sister chromatids apparently required for chiasma maintenance until anaphase I.


Genetics ◽  
1982 ◽  
Vol 101 (1) ◽  
pp. 81-89
Author(s):  
Adelaide T C Carpenter ◽  
Bruce S Baker

ABSTRACT The effects of eight recombination-defective meiotic mutants on crossing over within the X heterochromatin were examined. Since none permit substantial frequencies of exchange within heterochromatin although six lessen or abolish constraints on the location of exchanges within euchromatin, the systems that prohibit exchange within heterochromatin and that govern where exchanges will occur in euchromatin are under separate genetic control.—A minor component of the effects of mei-218 is the production of nonhomologous exchanges; of mei-9 is the recovery of deleted chromatids; and of mei-41 is the recovery of deleted chromatids and/or a low frequency of heterochromatic exchanges.


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