THE FREQUENCY OF ALLELIC LETHALS AND COMPLEMENTATION MAPS IN NATURAL POPULATIONS OF DROSOPHILA MELANOGASTER FROM MEXICO. Victor M.

Similar documents
Local and Seasonal Variations of Lethal Frequencies. Natural Populations of Drosophila melanogaster. Sumlo MINAMORI and Yoshlnori

61A the flies were mass-mated in half-pint culture bottles containing the usual

T drift in three experimental populations of Drosophila melanogastar, two

Rare male mating advantage in Drosophila melanogaster.

Linkage Mapping in Drosophila Melanogaster

INCREASING TREND IN FREQUENCIES OF LETHAL AND SEMILETHAL CHROMOSOMES IN A NATURAL POPULATION OF

A gene is a sequence of DNA that resides at a particular site on a chromosome the locus (plural loci). Genetic linkage of genes on a single

COMPARATIVE BEHAVIOURAL ANALYSIS OF MATING BETWEEN YELLOW AND WILD TYPE DROSOPHILA OF MELANOGASTER SPECIES GROUP

.might have been expected to be influenced by the spindle fibre were not. (standard map7). CROSSING-OVER IN DROSOPHILA

The Determination of the Genetic Order and Genetic Map for the Eye Color, Wing Size, and Bristle Morphology in Drosophila melanogaster

RELATIVE FREQUENCIES OF THE SEX-RATIO INVERSION IN NATURAL POPULATIONS OF Drosophila pseudoobscura FROM MEXICO. Víctor M. SALCEDA

ELIMINATION OF MUTANT TYPES IN SELECTION EXPERIMENT BETWEEN WILD TYPE AND MUTANT EYE COLOUR IN DROSOPHILA ANANASSAE

Example: Colour in snapdragons

Chromosomal assignment of the genetic factor, tu-91k, responsible for a melanotic tumour in the Drosophila melanogaster adult female

Experiment 1. The aim here is to understand the pattern of

The Effect of Temperature on the Viability of Superfemales in Drosophila melanogaster. Th. Dobzhansky

Figure 1: Transmission of Wing Shape & Body Color Alleles: F0 Mating. Figure 1.1: Transmission of Wing Shape & Body Color Alleles: Expected F1 Outcome

THE GENETIC FACTORS ALTERED IN HOMOZYGOUS. Manuscript received October 25, 1985 Revised copy accepted July 26, 1986

Inheritance of Aldehyde Oxidase in Drosophila melanogaster

Laboratory. Mendelian Genetics

ELECTRONIC APPENDIX. This is the Electronic Appendix to the article

Drosophila melanogaster. Introduction. Drosophila melanogaster is a kind of flies fruit fly that is widely used in genetic

Biology 164 Laboratory

Manuscript received May 23, 1974 Revised copy received September 10,1974 ABSTRACT

MECHANISM OF THE ORIGIN OF X-RAY INDUCED NOTCH. Summary.-Comparison has been made, using salivary gland chromosomes,

Incomplete Dominance

Biology 105: Introduction to Genetics Midterm EXAM. Part1. Definitions. 1 Recessive allele. Name. Student ID. 2 Homologous chromosomes

DISTRIBUTIVE PAIRING: MECHANISM FOR SEGREGATION OF COMPOUND AUTOSOMAL CHROMOSOMES IN OOCYTES OF DROSOPHILA MELANOGASTERl E. H.

Ch 8 Practice Questions

Section 8.1 Studying inheritance

X Chromosome Inversions and Meiosis in Drosophila melanogaster. G. W. Beadle, and A. H. Sturtevant

Chapter 15: The Chromosomal Basis of Inheritance

MELANOGASTER. Bridges, C Triploid Intersexes in Drosophila melanogaster. Science, NS, 54: E S P

This document is a required reading assignment covering chapter 4 in your textbook.

Name: PS#: Biol 3301 Midterm 1 Spring 2012

SIMULATION OF GENETIC SYSTEMS BY AUTOMATIC DIGITAL COMPUTERS III. SELECTION BETWEEN ALLELES AT AN AUTOSOMAL LOCUS. [Manuscript receit'ed July 7.

FURTHER DATA ON THE OVERDOMINANCE BRUCE WALLACE. Received December 8, 1962

Meiotic Transmission of Drosophila pseudoobscura Chromosomal Arrangements

Pedigree Construction Notes

Genetic analysis of sex-chromosome arrangement in Drosophila americana; a laboratory exercise for undergraduate or advanced placement students.

Chapter 15 - The Chromosomal Basis of Inheritance. A. Bergeron +AP Biology PCHS

mouse, which show a combination of unusual properties. The

GENETICS - NOTES-

Biology Department, University of North Carolina, CB# 3280, Coker Hall, Chapel Hill, North Carolina

Male Remating in Drosophila ananassae: Evidence for Interstrain Variation in Remating Time and Shorter Duration of Copulation during Second Mating

THE TEMPERATURE RESPONSES OF FLIES WITH THE DEFICIENCY VESTIGIAL-DEPILATE IN DROSOPHILA MELANOGASTER

Contributions to the Knowledge of Non-Disjunction of the Sex-Chromosomes in Drosophila virilis. I. General Problems

By Mir Mohammed Abbas II PCMB 'A' CHAPTER CONCEPT NOTES

Single Gene (Monogenic) Disorders. Mendelian Inheritance: Definitions. Mendelian Inheritance: Definitions

Lab 5: Testing Hypotheses about Patterns of Inheritance

Exam #2 BSC Fall. NAME_Key correct answers in BOLD FORM A

Chapter 15: The Chromosomal Basis of Inheritance

Epistasis among Drosophila persimilis Factors Conferring Hybrid Male Sterility with D. pseudoobscura bogotana

Relationship Between Various Chromosomal Changes. By M. Demerec Carnegie Institution of Washington, Cold Spring Harbor, N. Y., U. S. A.

A occurring X-chromosome known as the sex-ratio (SR) chromosome (LAK-

Heredity. Biology 30i Cooper

Downloaded from Chapter 5 Principles of Inheritance and Variation

Mendel s Methods: Monohybrid Cross

Genetics Practice Problems

Double The Muscle: Genotype and Probability

Pedigree Analysis Why do Pedigrees? Goals of Pedigree Analysis Basic Symbols More Symbols Y-Linked Inheritance

Characterization of a New Male Sterile Mutant in Watermelon

Lab Activity 36. Principles of Heredity. Portland Community College BI 233

THE GENETIC POPULATION STRUCTURE OF BRAZILIAI\' DROSOPHILA WILLISTONII

draw and interpret pedigree charts from data on human single allele and multiple allele inheritance patterns; e.g., hemophilia, blood types

Test Booklet. Subject: SC, Grade: HS Genetics Assessment. Student name:

X-RAY INDUCED MUTATIONS IN SPERMATOGONIAL CELLS OF DROSOPHILA AND THEIR DOSE-FREQUENCY RELATIONSHIP1

Class XII Chapter 5 Principles of Inheritance and Variation Biology

Downloaded from

SEX. Genetic Variation: The genetic substrate for natural selection. Sex: Sources of Genotypic Variation. Genetic Variation

Chapter 5 A Dose Dependent Screen for Modifiers of Kek5

I abnormal growths in the head of Drosophila melanogaster was discussed.

GONADAL MOSAICISM AS A FACTOR IN DETERMINING THE RATIO OF VISIBLE TO LETHAL, MUTATIONS IN DROSOPHILA'

BIOLOGY - CLUTCH CH.15 - CHROMOSOMAL THEORY OF INHERITANCE

DROSOPHILA PAULISTORUM GROUP1. The Rockefeller Uniuersity, New York City. Received March 17, 1971

THE INFLUENCE OF LIGHT ON GENE FREQUENCY CHANGES IN LABORATORY POPULATIONS OF EBONY AND NON-EBONY DROSOPHILA MELANOGASTER M. E.

UNIT 6 GENETICS 12/30/16

Nori Nakamura RERF consultant

Principles of Inheritance and Variation

Does Mendel s work suggest that this is the only gene in the pea genome that can affect this particular trait?

THE TETRASOMIC FOR CHROMOSOME 4 IN DROSOPHILA MELANOGASTER

Take a look at the three adult bears shown in these photographs:

WHAT S IN THIS LECTURE?

Polygenic Mutation in Drosophila melanogaster: Genetic Analysis of Selection Lines

IB BIO I Genetics Test Madden

What we mean more precisely is that this gene controls the difference in seed form between the round and wrinkled strains that Mendel worked with

Psych 3102 Lecture 3. Mendelian Genetics

The Chromosomal Basis of Inheritance

SALSA MLPA KIT P050-B2 CAH

C) Show the chromosomes, including the alleles on each, in the F1 hybrid progeny at metaphase of Meiosis 1 and mitosis.

The laws of Heredity. Allele: is the copy (or a version) of the gene that control the same characteristics.

Name Class Date. KEY CONCEPT The chromosomes on which genes are located can affect the expression of traits.

Week 4 Day 1 Lab: MENDELIAN TRAITS and INHERITANCE

The Modern Genetics View

QB365 Important Questions - Principles of Inheritance and Variation

Meiotic drive and evolution of female choice

Gallery Walk. Fundamentals of Genetics

PRINCIPLES OF INHERITANCE AND VARIATION

H lethal or semilethal in homozygotes, is very common in natural

Transcription:

UDC 575.2: 595.773.4 Original scientific paper THE FREQUENCY OF ALLELIC LETHALS AND COMPLEMENTATION MAPS IN NATURAL POPULATIONS OF DROSOPHILA MELANOGASTER FROM MEXICO Victor M. SALCEDA Departamento de biologia, Instituto nacional de investigaciones nucleares. Apartado Postal 18-1027, México, 11801, D.F. Mexico Salceda V.M. (2004): The frequency of allelic lethals and complementation maps in natural populations of Drosophila melanogaster from Mexico. Genetika, Vol. 36, No. 3, 205-212. Departing from a previous study on the genetic loads affecting the second chromosome of Drosophila melanogaster in four natural populations, 171 lethal chromosomes were recovered and maintained as a balanced stocks in the condition Cy L / l (l=lethal); of those lethals 24 correspond to population A, 50 to populations B and C and 47 to population D. later on an intra-population allelism test for the four populations was performed for each one. A total of 3807 inter lethal crosses were done yielding a total of 110 allelic combinations, from them the respective percentage of allelism for each population was calculated and they are as follow: 3.98 % for population A, 1.80 % for population B, 3.67 % for population C and 2.96 % for population D. the observed values for the frequency of allelism in these populations are not significantly different from those reported by other authors in similar studies in natural and/or experimental populations. Beside these values the frequency for singles, doubles, triplets and even quadruplets present in each population were determined, they shown the presence of various complementation maps due to the clustering of few different lethals; also a large complementation map formed by a large cluster involving the presence of 26 different Corresponding author: Victor M. Salceda, Departamento de biologia, Instituto nacional de investigaciones nucleares. Apartado Postal 18-1027, México, 11801, D.F. Mexico. e-mail: vmss@nuclear.inin.mx

206 GENETIKA, Vol. 36, No. 3, 205-212, 2004. lethals found in population D all of them combined constituting a single unit was found. Key words: genetic load, allelism, complementation map, Drosophila INTRODUCTION It is well known that in natural populations of Drosophila a significant portion of the variability consists of lethal or deleterious genes concealed in the heterozygous state. Studies have been carried out in natural populations in many countries to reveal the presence and extent of such variability by means of making homozygous the recessive lethal/deleterious gene and noting the absence/reduction in the class compared with its normal recovery (e.g., WALLACE, 1950, in the U.S, PAIK and SUNG, 1969, in Korea, and SALCEDA, 1977, in Mexico). moreover, when identified lethals are intercrossed with one another, information regarded allelism is obtained. Results of such studies provide the basis for estimates regarding the persistence of different lethal genes over time (YTTERBORN, 1971), distances between different populations (OSHIMA and WATANABE, 1967; 1968a, b). By making assumptions regarding the rate at which a locus is capable to mutate to a recessive lethal in doing so, DOBZHANSKY and WRIGHT (1941), WRIGHT et al. (1942) and IVES (1945) arrived at estimates of the frequency of allelic lethals in Drosophila pseudoobscura and D. melanogaster, respectively. In the present study, the work of SALCEDA (1977) on natural populations of D. melanogaster in Mexico City was expanded by including other population, that of "La Nopalera" in the near by State of Mexico. A total of 171 recessive lethals isolated from those four populations is the subject of this study. Tests for allelism in these populations showed a range value from 1.80-3.98 % with an average of 3.03%, not very different from previous reports in the literature for D. melanogaster populations in other countries. The study involves also a complementation analysis of those complex clusters of lethal genes that appeared in the test. MATERIAL AND METHODS A series of recessive lethal genes were recovered from natural populations of D. melanogaster in four different localities: three of them in the southern area of Mexico City, separated by no more than 6 km from each other, the remained one is located in the near by State of Mexico at approximately 40 km of the other sites. The populations are designated from the place of collection as follow: A:-"La Nopalera", B.-"Mixcoac", C.-"Colonia del Valle" and D.-"Coyoacán". The lethals were maintained as stocks balanced against a chromosome bearing Ins (2L+2R), Cy,L. Lethal bearing strains from each population were numbered as they were recovered from the populations and correspond 1-50 for each populations B and C, 1-43 for population D and 1-24 for population A. Males and virgin females were collected and the following mating protocol used: from any

V.M.SALCEDA: LETHAL ALLELIC FREQUENCIES AND COMPLEMENTATION MAP 207 given population, 3-5 Cy L / l(l for lethal) females from strain 1 were crossed to 3-5 Cy L / l males of strains 2,3,4, etc. to the last numbered strain in that population; and 3-5 Cy L / l females from strain 2 were mated with 3-5 Cy L / l males from strains 3,4,5,etc. Until all possible combinations were achieved. Approximately 100 crosses of Cy L / l x X Cy L / l + were made daily. After 12-14 days from the inception of the cross, the F1 progeny were examined for the presence/absence of the non-cy L class, its presence indicating nonallelism, its absence taken as evidence of allelism. During the analysis some clusters appeared and they were analyzed as follow: the absence of allelism indicates a single lethal, if two of them are allelic the pair forms a double, if three are allelic among them they constituted a triplet and so on. Now in some cases for one of the lethals that form a double is also allelic with one of the members of another pair then the two doubles constitute a cluster; for instance: lethal 1 is allelic with lethal 8 forming one double, and lethal 5 is allelic with 8 lethal but lethal pair 1 and 5 are non allelic it means that the locus represented by 5 lethals, shares its action partially with 1 and 8 and together complement the action of that locus. This rationale was followed in all similar cases in order to build the several complementary loci or clusters. All the experiments were carried out at a temperature of 24+ 1ºC, and the cultures maintained in 1/4 pint bottles, using as a food the corn meal-agar-sugar-yeast medium of regular use in the laboratory. RESULTS AND DISCUSSION A summary of the results of the tests for allelism among the 171 lethals belonged to the four populations is given in Table 1. Table 1. Allelic frequencies of lethal genes in four natural populations of Drosophila melanogaster from Mexico Population A B C D Total Strains tested 24 50 50 47 171 # crosses 276 1225 1225 1081 3807 allelic crosses 11 22 45 32 110 % allelism 3.98 1.80 3.67 2.96 2.90 Details of the results of inter-strain crosses within each population is shown in Fig. 1 and 2 for populations A-D, where a black square indicates a presumed allelic combination. A total of 3807 inter-strain crosses were carried out. Of these, 110 failed to produce non-cy flies indicating they are alleles and given a mean of 3.03% allelism. Specifically, in populations B and C (50 lethals tested in each), where allelic frequencies of 1.80% and 2.96%, respectively were found; in population D (47 lethals tested), with a 2.96% allelism and in population A (24 lethals tested), with a 3.98% allelism these values are not very different from those found previously by others which fell in the range 2-6% found anywhere. For ex-

208 GENETIKA, Vol. 36, No. 3, 205-212, 2004. ample, with regard to studies in D. melanogaster, an allelic frequency of 4.07% was found in a population in Bogota (Wallace, 1950), 1.95-6.44% for Japanese populations (Oshima, 1969), and values of 2.72% and 2.38% for 2 Korean populations (Paik and Sung, 1969). For D. pseudoobscura Wright et al (1942) reported an allelic frequency of 2.04%. Fig. 1. Allelism test for lethals in natural populations of Drosophila melanogaster, populations La Nopalera below, Mixcoac above. The graphic representation of the results from the crosses (Fig. 1 and 2) allows an analysis of the clustering of lethal genes. For example (figure 1 above) lethals 1, 7 and 23 were found to be allelic among them, it means that the three of them correspond to the same locus and therefore are alleles; now following the same rationale for the complete sample we could classify the lethal genes in singles, doubles, triples, etc., according to the number of lethal stocks involved. From these analyses we were able to get the following results: from population "La Nopalera" (figure 1 below) we analyzed 24 lethals, as a result of the test, 10 demonstrated to be singles and appeared 11 allelic crosses arranged in the following way: two doubles "A" and "B" represented one pair by the lethals 8-10 and the other by lethals 17-22; one triplet "C" combination formed by the lethals 7, 15 and 19; and the "D" cluster product of the linkage between the doublet 6-11, the triplet 11-18-23 and the quadruplet 5-14-23-24. In the case of population B, "Mixcoac", the analysis is based on 50 lethals of which 23 are singles; the test produced 22 allelic crosses being doubles the following pairs "A"3-45,"B 12-33 and "C" 25-29; the triplets constituted by the triads "D" 1-7-23, "E" 4-13-18, "F" 10-14-19, "G" 32-36-43 and "H" 35-37-38 as well as

V.M.SALCEDA: LETHAL ALLELIC FREQUENCIES AND COMPLEMENTATION MAP 209 a quintuplet "I" with the lethals 20-26-27-30-46. The combinations double-double or double-triplet produced the complemented clusters "D", "G", "H" and "I" in different combinations. Fig. 2. Alelism test for lethals in natural populations of Drosophila melanogaster, populations Colonia del Valle below, Coyoacan above. In the same way 50 lethals from population C "Colonia del Valle" gave as a result the presence of 17 singles and 45 allelic crosses forming 12 doubles, 4 triplets 2 quadruplets, 2 quintuplets 1 sextuple and one constituted by 7 lethals, due to the presence of complementation made the formation of actually 8 doublets(4-9), (7-20), (11-34), (13-18), (14-24), (19-44), (27-28) and (30-40), the triplet (10-22-50) and a cluster involving different combinations between doubles and/or triplets. Here is important to point out that eventually A = B, B=C but A is not equal to C as it is seen in several cases in this population. 28 32 44 41 40 35 32 42 41 10 6 41 37 35 34 33 25 10 47 44 38 37 36 34 37 36 34 20 34 20 47 44 38 37 36 34 40 47 31 39 40 29 39 40 11 8 15 24 29 40 16 15 24 Fig. 3.- Graphic representation of a cluster involving 26 different lethal genes in a natural population of Drosophila melanogaster.

210 GENETIKA, Vol. 36, No. 3, 205-212, 2004. Finally population D "Coyoacán" showed to be the most complex one since out of 47 lethals analyzed 19 were singles, the test give as a result the presence of 32 allelic combinations and from them only one was a double, the remaining 26 lethals are present in doubles, triplets and quadruples as a separate groups but all together constituting a unique cluster involving the 26 lethals, this case schematically looks as seen in Fig. 3. CONCLUSION From the results shown we could infer that the frequency of allelism among the four populations analyzed that they did nor differ significantly from those reported by several authors and that thy constitute small clusters inside the same locus, these clusters involve either 2, 3 or 4 different lethas all of them corresponding to the same locus even if they are partially connected with each other; in the same way a large cluster in population D suggests the presence of a complementation among the different participants, 26 of them, and allowed us to built a corresponding complementation map, it in some cases the partial contributors represent small pieces of 2-5 lethals all of them belonging to the same locus with partial contributions. Acknowledgments: The author wishes to express his thanks to Prof. Stanley Zimmering for kindly review the typescript as well his suggestions also to Prof. Dragoslav Marinkovic for prepare the Serbian version of the abstract. Received November 15 th, 2004. Accepted December 27 th, 2004. REFERENCES DOBZHANSKY T.H. and S. WRIGHT. (1941): Genetics of natural populations. V. Relation between mutation rates and accumulation of lethals in populations of Drosophila pseudoobscura. Genetics 26, 23-51. IVES P.T. (1945): The genetic structure of American populations of Drosophila melanogaster. Genetics 30, 167-196. OSHIMA C. and T.K. WATANABE. (1967): Allelic rates between lethal genes extracted from Japanese natural populations of Drosophila melanogaster. Natl. Inst. Gen. Japan 18, 76-77. OSHIMAC. and T.K. WATANABE. (1968): Allelic relation between lethal genes distributed in natural populations. Natl. Inst. Gen. Japan 19, 54-55. OSHIMA C. and T.K. WATANABE. (1968b): Relationship between the dispersal of flies and the frequency of allelism of lethals in natural populations. Natl. Inst. Gen. Japan 19, 55-57. PAIK Y.K. and K.C. SUNG. (1969): Behavior of lethals in Drosophila melanogaster populations. Japan. J. Genetics vol. 44. Suppl. 1, 180-192. SALCEDA V.M. (1977): Carga genética en siete poblaciones naturales de Drosophila melanogaster (Meigen) en diferentes localidades de México. Agrociencia 28, 47-52.

V.M.SALCEDA: LETHAL ALLELIC FREQUENCIES AND COMPLEMENTATION MAP 211 WALLACE B. (1950): Allelism of second chromosome lethals in Drosophila melanogaster. Proc. Nat. Acad. Sci. 36, 654-657. WRIGHT S., T.H. DOBZHANSKY, and W. HOVANITZ. (1942): Genetics of natural populations. VII. The allelism of lethals in the third chromosome of Drosophila pseudoobscura. Genetics 27, 363-394. YTTERBORN K. H. (1971): Influence of the population genetic background on the persistency of a recessive lethal in Drosophila melanogaster. Genet. Res. Camb. 17, 103-111.

212 GENETIKA, Vol. 36, No. 3, 205-212, 2004. UČESTALOST LETALNIH ALELA I KOMPLEMENTACIONIH MAPA U PRIRODNIM POPULACIJAMA DROSOPHYLA MELANOGASTER IZ MEKSIKA V. M. SALCEDA Odsek za biologiju, Nacionalni Institut za citološka istraživanja. Apartado Postal 18-1027, Meksiko, 11801, D.F. Meksiko Izvod Polazeći od prethodnih studija genetičkog opterećenja na drugom hromozomu kod Drosophyla melanogaster, u četiri prirodne populacije, otkrivena su 171 letalna hromozoma i održavana kao faktor ravnoteže u uslovima Cy L/1 (1= letalan); od ovih letalnih 24 odgovaraju populaciji A, 50 populaciji B i C a 47 populaciji D. Vršena su ispitivanja testom intra-populacionog alelizma za sve četiri populacije. Izvršena su 3807 inter - letalna ukrštanja i dobijeno je ukupno 110 alelnih kombinacija. Izračunat je procenat alelizma za svaku populaciju i to: 3,98 % za populaciju A; 1,80 % za populaciju B; 3,67 % za populaciju C i 2,96 % za populaciju D. Dobijene vrednosti za učestalost alela u ispitivanim populacijama ne razlikuju se značajno od vrednosti koje su dobili drugi autori sličnim spitivanjima u prirodnim ili eksperimentalnim istraživanjima. Pored ovih vrednosti za učestalost, kada je utvrđeno je prisustvo singlova, dupleta, tripleta ili kvaddripleta u svakoj populaciji, pokazano je prisustvo različitih mapa komplementacije zbog grupisanja nekoliko različitih letalnih alela; velika mapa komplementacije, formirana od velikog klastera (grupe) koji uključuje 26 različitih letala, nađena je u populaciji D, što ukazuje da je, kao posledica kombinovanja svih, konstituisana jedna jedinica. Primljeno 15. XI 2004. Odobreno 27. XII 2004.