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Remembering the past – studies on evolution done by the genetics group at Universidade Federal do Rio Grande do Sul (UFRGS)

Abstract

After a brief introduction about the factors that are involved in science development, and world and Brazilian evolutionary genetics, the studies developed in Porto Alegre in this area were reviewed. Four periods in the development of this group were distinguished: (a) Origins and first expansion (1949-1961); (b) Second expansion (1962-1988); (c) Third expansion (1989-2001); and (d) The last 15 years (2002-present). The international Porto Alegre Biological Evolution Workshops (PABEWs), with five biannual events from 2007 o 2015, were also mentioned. The final message stressed the importance of the maintenance of this and other Brazilian groups of research through adequate finance and recognition.

Keywords:
History; genetics research; evolutionary genetics; Porto Alegre; Brazil

Factors involved in science development

What conditions the formation and maintenance of a research group? We could conveniently classify them in two components. The first is environmental. Important scientific investigation cannot thrive in a hostile environment, characterized by violence (wars, within-nations arrest due to power contests), poor economic development, or general ignorance about the importance of science. The second is mainly historical; it depends on the presence of the right person, in the right place. All societies have persons endowed with high intelligence and adequate drive to pursue a successful scientific career. However, they may never have the opportunity of adopting it due to the absence of adequate conditions. Another crucial factor is continuity. Initially favorable situations may be of short duration, and the entire enterprise may then fail to be maintained. In addition, the formation of a scientist is a slow process. It depends on an initial adequate interpersonal relationship in the educational process, which is of an artisan type. The assimilation of the abstract concepts involved requires time and may be subjected to distracting interests. Therefore, research groups lasting for many years are rarely numerous.

It is in this context that we should view the history of our group that, despite fluctuations in the economic conditions and governmental policies, maintained a pattern of excellence not common in Third World countries. This continuity can be documented through the years that elapsed since Doctoral titles were awarded to the main contributors of our research group (Table 1). The dates extend from 1954 to 2009, more than half a century, with a steady rhythm of growth during the 1970s to 1990s.

Table 1
List of the main researchers involved in evolutionary studies in Porto Alegre with the dates they obtained their Ph.D. degrees1 1 Flavio Lewgoy never obtained a formal Ph.D. degree. .

World and Brazilian evolutionary genetics

The beginning of evolutionary genetics can be conveniently dated to 1908, when the fundamental principle developed by G. H. Hardy (1877-1947) and W. Weinberg (1862-1937), established what would be the fate of genes in populations. What could be labeled as the period of classical genetics extends from 1900 to 1953 (Carlson, 2004Carlson EA (2004) Mendel’s Legacy. The Origin of Classical Genetics. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, 332 pp.), and the formation of the UFRGS genetics group occurred during the fusion of Darwinism and Mendelism, in the fertile two decades (1930-1950) of the development of the synthetic theory of evolution (Herrera et al., 2016Herrera RJ, Garcia-Bertrand R and Salzano FM (2016) Genomes, Evolution, and Culture. Past, Present, and Future of Humankind. John Wiley & Sons, Chichester, 254 pp.).

The subsequent years were characterized by a phenomenal development in the area of genetics, starting in 1953 with the elegant DNA molecule model devised by James D. Watson (born in 1928) and Francis H. C. Crick (1916-2004), to which Rosalind E. Franklin (1921-1958) and Maurice H. F. Wilkins (1916-2004) significantly contributed.

The progress in the area of evolutionary genetics was in great part due to the development of laboratory and analytic methods for the study of population variability, that evolved from immunological to biochemical, to molecular determinations, that then were extensively analyzed by computer and bioinformatics programs.

What was happening in Brazil during these years? Well, no Brazilian received the Nobel Prize for his/her studies in evolutionary genetics. However, Brazilian researchers followed closely these tendencies, furnishing valuable data of worldwide importance. I have reviewed this information along the years (Salzano, 1979Salzano FM (1979) Estudo sobre a evolução biológica no Brasil. In: Ferri MG and Motoyama S (eds) História das Ciências no Brasil. Editora Pedagógica e Universitária e Editora da Universidade de São Paulo, São Paulo, pp. 241-264., 2011Salzano FM (2011) Recordar é Viver – História da Sociedade Brasileira de Genética. Sociedade Brasileira de Genética, Ribeirão Preto, 215 pp., 2012Salzano FM (2012) Genômica e Evolução – Moléculas, Organismos e Sociedades. Oficina de Textos, São Paulo, 271 pp.) and the reader is referred to these publications for more details.

Studies in Porto Alegre

Origins and first expansion (1949-1961)

It all started with a young man of 24 years of age, Antonio Rodrigues Cordeiro, student of the Natural History Course, School of Philosophy, University of Rio Grande do Sul (at the time it was not yet a Federal University). After a practical class on Drosophila melanogaster he decided to verify whether these flies occurred also in our environment. He then wrote to Crodowaldo Pavan, at the time an Assistant Professor at the University of São Paulo, who sent him a detailed letter on the way that these flies could be collected and raised in the laboratory.

One year later, Theodosius Dobzhansky, one of the scholars responsible for the development of the synthetic theory of evolution, arrived in São Paulo for a stay of one year, and Cordeiro, together with A. G. L. Cavalcanti (who worked in Rio de Janeiro) were selected for a one-year fellowship to form (with others) the team responsible for the research to be coordinated by Dobzhansky.

In September, 1949, A. R. Cordeiro returned from São Paulo. He was already an Assistant Professor at UFRGS, and with the decisive support of the then Director of the School of Philosophy, Bernardo Geisel (1901-1985), he organized a small laboratory in the basement of the Law School. The first expansion of genetics research in Porto Alegre occurred in 1953, when we moved to a new building with much more space, which was the seat of a newly created Institute, the Institute of Natural Sciences. During the period that elapsed until the new move, in 1961, significant research was performed, which is summarized in Cordeiro and Salzano (1961)Cordeiro AR and Salzano FM (1961) Histórico, Secção de Genética do Instituto de Ciências Naturais da Universidade do Rio Grande do Sul. Atas do 1º Simpósio Sul-Americano de Genética, pp 227-248..

My relationship with the group started as a voluntary student, before my graduation, in 1950. In the next year I received a fellowship from the University of São Paulo, and during one I year worked there under the guidance of Antonio Brito da Cunha, Crodowaldo Pavan, and Hampton L. Carson, from the Washington University, Missouri, USA. After returning to Porto Alegre in 1952 I was invited to work as an Instructor at UFRGS, the institution where I remained until now. Four years later (1956) I obtained a one-year post-doctoral fellowship to work at the University of Michigan, Ann Arbor, under the supervision of James V. Neel, and after my return started to work on human population genetics, that continues up to the present.

Selected aspects of the research in evolutionary genetics performed at the time will now be briefly summarized. Key persons involved besides Cordeiro and myself were, in alphabetical order of the first name, Casemiro V. Tondo, Edmundo K. Marques, Flavio Lewgoy, Helga Winge, and Marly Napp.

Recessive alleles concealed due to dominance in Drosophila could be detected due to a skillful method of crossings. These were performed by the group using Drosophila willistoni, and the main results were reported in Burla et al. (1949)Burla HA, da Cunha AB, Cordeiro AR, Dobzhansky Th, Malogolowkin C and Pavan C (1949) The willistoni group of sibling species of Drosophila. Evolution 3:300-314., Pavan et al. (1951)Pavan C, Cordeiro AR, Dobzhansky N, Dobzhansky Th, Malogolowkin C, Spassky B and Wedel M (1951) Concealed genic variability in Brazilian populations of Drosophila willistoni. Genetics 36:13-30., Cordeiro (1952)Cordeiro AR (1952) Experiments on the effects in heterozygous condition of second chromosomes from natural populations of D. willistoni. Proc Natl Acad Sci U S A 36:471-478., and Cordeiro and Dobzhansky (1954)Cordeiro AR and Dobzhansky Th (1954) Combining ability of certain chromosomes of Drosophila willistoni and invalidation of the “wild type” concept. Am Nat 88:75-86..

In 1956 the laboratories of biophysics and genetics merged, and Casemiro V. Tondo became a full member of the group. Cordeiro was aware of the need to develop new methods of genetic analysis, and together with Tondo and Flavio Lewgoy, a biochemist, produced a series of four articles all entitled Biophysical Genetics (Tondo and Cordeiro, 1956Tondo CV and Cordeiro AR (1956) Biophysical Genetics. I. Paper electrophoresis separation of the eye pigments and other components of Drosophila. Rev Bras Biol 16:519-526.; Lewgoy and Cordeiro, 1958Lewgoy F and Cordeiro AR (1958) Biophysical Genetics. II. Chromatographic analysis of homo and heterozygous strains of D. willistoni from natural populations. Rev Bras Biol 18:353-366.; Tondo et al., 1959Tondo CV, Lewgoy F and Cordeiro AR (1959) Biophysical Genetics. III. Spectrophotometric and electrophoretic studies of Drosophila red eye pigments and other components. Rev Bras Biol 19:367-378.; Cordeiro et al., 1960a)Cordeiro AR, Lewgoy F and Tondo CV (1960a) Biophysical Genetics. IV. Chromatographic patterns of Drosophila willistoni races, interracial hybrids and the heterosis phenomena. Rev Bras Biol 20:69-78.. They applied chromatography, paper electrophoresis, and spectrophotometric methods to characterize homo and heterozygous strains, as well as interracial hybrids of Drosophila willistoni.

Concomitantly, inversion polymorphisms and the peculiarities of the bocainensis cryptic group of species were investigated by Da Cunha et al. (1953)Da Cunha AB, Brncic D and Salzano FM (1953) A comparative study of chromosomal polymorphism in certain South American species of Drosophila. Heredity 7:193-202. and Salzano (1956)Salzano FM (1956) Chromosomal polymorphism and sexual isolation in sibling species of the bocainenses subgroup of Drosophila. Evolution 10:288-297.. The fate of chromosome inversions experimentally released in populations where they had been previously absent was examined by Cordeiro et al. (1960b)Cordeiro AR, Salzano FM and Marques VB (1960b) An interracial hybridization experiment in natural populations of D. willistoni. Heredity 15:35-45..

In another area, the first studies in plants were performed by Winge (1959)Winge H (1959) Studies on cytotaxonomy and polymorphism in the genus Alophia (Iridaceae). Rev Bras Biol 19:195-201., on the cytotaxonomy and polymorphism of the genus Alophia (Iridaceae).

Studies in human evolutionary genetics had started in 1958, and a series of papers reporting the investigations performed among the Kaingang Amerindians of Rio Grande do Sul were published (Salzano FM (1961a) Studies on the Caingang Indians. I. Demography. Hum Biol 33:110-130. Salzano FM (1961b) Studies on the Caingang Indians. II. Morphological characteristics. Z Morphol Anthropol 51:356-371. Salzano FM (1961c) Studies on the Caingang Indians. III. Blood groups. Am J Phys Anthropol 19:391-404. Salzano, 1961a-dSalzano FM (1961d) Rare genetic conditions among the Caingang Indians. Ann Hum Genet 25:123-130.).

Second expansion (1962-1988)

The transfer of the Department’s seat from the UFRGS Central Campus to a new and much expanded space, located in three floors of a commercial building situated in the center of the city, opened considerable new opportunities for expansion, both in terms of personnel and research.

Considering first studies in animals, the investigations with Drosophila continued with vigor; examples are as follows: 1. The finding of hybrids between D. willistoni and D. paulistorum (Winge and Cordeiro, 1963Winge H and Cordeiro AR (1963) Experimental hybrids between D. willistoni, Sturtevant and D. paulistarum, Dobzhansky and Pavan from southern marginal populations. Heredity 18:215-222.), first denied by some researchers, but afterwards firmly confirmed; 2. the question of the adaptation of D. willistoni to an environment with high background radiation (Cordeiro et al., 1973Cordeiro AR, Marques EK and Veiga-Neto AJ (1973) Radioresistance of a natural population of Drosophila willistoni living in a radioactive environment. Mutat Res 19:325-329.); 3. biochemical variability (esterases, alcohol dehydrogenases) in natural populations (Napp and Cordeiro, 1978Napp M and Cordeiro AR (1978) Genetic variability and disequilibrium in the major esterase locus in four species of the Cardini group of Drosophila. Rev Bras Genet 1:193-202.; Albuquerque and Napp, 1981Albuquerque CMR and Napp M (1981) Genetic variability at the esterase-6 locus in natural populations of Drosophila simulans in relation to environmental heterogeneity. Genetics 98:399-407.; Oliveira and Cordeiro, 1985Oliveira AK and Cordeiro AR (1985) Ontogenetic pattern of alcohol dehydrogenase in the sibling species D. melanogaster and D. simulans. Rev Bras Biol 45:471-479.; Uriarte and Napp, 1988Uriarte TL and Napp M (1988) Environmental factors, numerical fluctuations and the variation of the EST-3 active and null allele frequencies in natural populations of Drosophila griseolineata. Rev Bras Genet 11:827-838.); 4. ecology in D. incompta (Hofmann and Napp, 1984Hofmann PRP and Napp M (1984) Genetic-environmental relationships in Drosophila incompta, a species of restricted ecology. Rev Bras Genet 7:21-39.); and 5. chromosomal polymorphism in D. willistoni (Valente and Araújo, 1986Valente VLS and Araújo AM (1986) Chromosomal polymorphism, climatic factors and variation in population size of Drosophila willistoni in southern Brazil. Heredity 57:149-160.). Studies on the butterfly genus Heliconius were performed by Lima and Araújo (1982)Lima FAM and Araújo AM (1982) Studies on the genetics and ecology of Heliconius erato (Lepidoptera, Nymphalidae). II. Inheritance of esterases and genotypic distribution in a natural population. Rev Bras Genet 5:679-686., and Menna-Barreto and Araújo (1985)Menna-Barreto Y and Araújo AM (1985) Evidence for host plant preferences in Heliconius erato phyllis from southern Brazil (Nymphalidae). J Res Lepidopt 24:41-46.. Going from insects to mammals, investigations were done on Scapteromys (Freitas et al., 1984Freitas TRO, Mattevi MS and Oliveira LFB (1984) Unusual C-bands patterns in three rearranged karyotype forms of Scapteromys (Rodentia, Cricetidae) from Brazil. Cytogenet Cell Genet 38:39-44.), Nectomys (Maia et al., 1984Maia V, Yonenaga-Yassuda Y, Freitas TRO, Kasahara S, Mattevi MS, Oliveira LFB, Galindo MA and Sbalqueiro IJ (1984) Supernumerary chromosomes, Robertsonian rearrangements and variability of the sex chromosomes of Nectomys squamipes (Cricetidae, Rodentia). Genetica 63:121-128.), and Deltamys (Sbalqueiro et al., 1984Sbalqueiro IJ, Mattevi MS and Oliveira LFB (1984) A X1X1X2X2/X1X2 Y mechanism of sex determination in a South American rodent species (Deltamys kempi). Cytogenet Cell Genet 38:50-55.). Also, a long-term relationship between the Genetics Departments of the Federal Universities of Rio Grande do Sul and Pará resulted in four articles about the genetic variability of Amazonian buffaloes and non-human primates (Cebus, Alouatta). Details can be obtained with Horacio and Maria Paula Cruz Schneider, in Belém.

Plant evolutionary genetics involved: 1. Chromosome relationships in the genera Paspalum and Axonopus (Gramineae), (Moraes-Fernandes et al., 1968Moraes-Fernandes MIB, Barreto IL and Salzano FM (1968) Cytogenetic, ecologic and morphologic studies in Brazilian forms of Paspalum dilatatum. Can J Genet Cytol 10:131-138., 1973Moraes-Fernandes MIB, Barreto IL and Salzano FM (1973) Cytogenetic, ecologic and morphologic studies in Brazilian forms of Paspalum notatum. Can J Genet Cytol 15:523-531., 1974Moraes-Fernandes MIB, Barreto IL, Salzano FM and Sacchet AMOF (1974) Cytological and evolutionary relationships in Brazilian forms of Paspalum (Gramineae). Caryologia 27:455-465.; Hickenbick et al., 1975Hickenbick MCM, Vals JFM, Salzano FM and Moraes-Fernandes MIB (1975) Cytogenetic and evolutionary relationships in the genus Axonopus (Gramineae). Cytologia 40:185-204.); 2. Altitude and cyanogenesis in the white clover Trifolium repens (Araújo, 1976Araújo AM (1976) The relationship between altitude and cyanogenesis in white clover (Trifolium repens L.). Heredity 37:291-293.); and 3. Biochemical variability in the rubiacea Relbunium (Porto et al., 1977Porto ML, Mariath JEA, Detoni ML, Cavalli SS, Winge H and Ehrendorfer F (1977) The systematics and evolution of the genus Relbunium (Rubiaceae). I. New species of Relbunium (Rubiaceae) from Brazil with notes on flavonoid patterns. Plant Syst Evol 128:177-193.; Cavalli-Molina and Winge, 1988Cavalli-Molina S and Winge H (1988) Phenetic relationships among populations of the autogamous plant Relbunium hypocarpium. Rev Bras Genet 11:401-418.).

Extensive work during this period was done on human populations, and the corresponding list of publications is too extensive to be given in full. Key persons at this time were (again by alphabetical listing of the first name) Casemiro V. Tondo, Fernando J. da Rocha, Mara H. Hutz, Maria Helena L. P. Franco, Maria José de Melo e Freitas, Sidia M. Callegari-Jacques, and Tania A. Weimer. I published studies resulting from field work on Amerindians, including the Kaingang, Xavante, Kayapo, Krahó, Macushi, Wapishana, Yanomama, Ticuna, Pacaás Novos, Sateré-Mawé, and Içana River populations. These studies, together with others done by our group and by additional researchers, were considered in a global way by Salzano and Callegari-Jacques (1988)Salzano FM and Callegari-Jacques SM (1988) South American Indians: A Case Study in Evolution. Oxford University Press, Oxford, 259 pp.. Non-Amerindian populations were also investigated, including communities from Porto Alegre, Natal, Aracajú, and several Amazonian locations. Special mention should be made of the discovery of Hemoglobin Porto Alegre (Tondo et al., 1963Tondo CV, Salzano FM and Rucknagel DL (1963) Hemoglobin Porto Alegre, a possible polymer of normal hemoglobin in a Caucasian Brazilian family. Am J Hum Genet 15:265-279.) due to its peculiarity (in vitro polymerization into octamers and dodecamers), as well as by its intermediate frequency, not being very rare nor much frequent. These results, together with those presented in the context of the next historical period, were reviewed in Salzano and Bortolini (2002)Salzano FM and Bortolini MC (2002) The Evolution and Genetics of Latin American Populations. Cambridge University Press, Cambridge, 512 pp..

Third expansion (1989-2001)

With the increase in the number of persons and studies that occurred in this and the following period, references would have to be even more selective than those of the previous sections. Starting with animal evolutionary genetics, 12 articles reporting Drosophila results have been published; including D. nebulosa, D. maculifrons, D. willistoni, D. paulistorum, D. simulans, D. polymorpha, D. tripunctata, and many other species. A general review about the transposable elements in Neotropical Drosophila was published by Loreto et al. (1998)Loreto ELS, Basso da Silva L, Zaha A and Valente VLS (1998) Distribution of transposable elements in Neotropical Drosophila. Genetica 101:417-428.. Work on other insects were much less numerous, including aphids, Chauliognathus (Coleoptera), and Dryas iulia (Lepidoptera; Haag et al., 1993Haag KL, Araújo AM and Zaha A (1993) Genetic structure of natural populations of Dryas iulia (Lepidoptera, Nymphalidae) revealed by enzyme polymorphism and mtDNA RFLP. Biochem Genet 31:449-460.). Studies in rodents were numerous, involving work on Deltamys, Ctenomys, Oryzomys, Oligoryzomys, Akodon, Rhipidomys, Delomys, Nectomys, and Decomys genera, as well as two species of bats and Neotropical cats (Eizirik et al., 1998Eizirik E, Bonatto SL, Johnson WE, Crawshaw PG, Vie JC, Brousset DM, O’Brien SJ and Salzano FM (1998) Phylogeographic patterns and evolution of the mitochondrial DNA control region in two Neotropical cats (Mammalia, Felidae). J Mol Evol 47:613-624.). The association between the Federal Universities of Pará and Rio Grande do Sul (see the previous section) resulted in nine articles published between 1989 and 1995 on biochemical protein polymorphisms, and seven on chromosome markers, all in New World primates. Details about this latter data set can be obtained from Julio Cesar Pieczarka and/or Cleusa Y. Nagamachi in Belém.

In plants, additional studies in Relbunium, Ilex, and Leucaena (Leguminosae; Cardoso et al., 2000Cardoso MB, Schifino-Wittmann MT and Bodanese MH (2000) Taxonomic and evolutionary implications of intraspecific variability in chromosome numbers of species of Leucaena Benth (Leguminosae). Bot J Linn Soc 134:549-556.) were published.

As far as humans are concerned, as mentioned previously, the results obtained on non-Amerindian populations were extensively reviewed in Salzano and Bortolini (2002)Salzano FM and Bortolini MC (2002) The Evolution and Genetics of Latin American Populations. Cambridge University Press, Cambridge, 512 pp.. Special mention can be made of a series of articles that resulted from a joint program of our group with the Biological Anthropology Department, School of Humanities and Education Sciences, Universidad de la República, Montevideo, as for the study by Sans et al. (1997)Sans M, Salzano FM and Chakraborti R (1997) Historical genetics in Uruguay: Estimates of biological origins and their problems. Hum Biol 69:161-170.. This period was especially fruitful with regard to the genetic investigations on Amerindian populations, performed in association with a network of colleagues from Latin America, North America, Europe and Asia. No less than 47 different groups (Table 2) were investigated on various aspects related to protein and DNA markers. Details can be provided on request. Two especially important, widely cited papers were those of Bonatto and Salzano (1997aBonatto SL and Salzano FM (1997a) A single and early migration for the peopling of the Americas supported by mitochondrial DNA sequence data. Proc Natl Acad Sci U S A 94:1866-1871., bBonatto SL and Salzano FM (1997b) Diversity and age of the four major mtDNA haplogroups and their implications for the peopling of the New World. Am J Hum Genet 61:1413-1423.) who, through a sophisticated analysis of Amerindian mitochondrial DNA sequences, arrived at the conclusion that the prehistoric peopling of the Americas occurred due to a single and early migration.

Table 2
List of the Amerindian populations for which genetic data have been reported by members of the Porto Alegre group in collaboration with many colleagues from Latin America, North America, Europe, and Asia, in the period between 1989 and 2001.

The last 15 years (2002-present)

The amount of publications presented in this period is very large, and a comprehensive list is impossible within the limits of this review. Therefore, only general information is provided in Tables 3-6, with indications of the years in which they were published and the colleagues who could give more details about them.

Table 3
Selected examples of evolutionary studies of a general nature and on microorganisms performed by members of the Porto Alegre group (2002-present).
Table 4
Selected examples of plant evolutionary studies performed by members of the Porto Alegre group (2002-present).
Table 5
Selected examples of animal evolutionary studies performed by members of the Porto Alegre group (2002-present).
Table 6
Selected examples of human evolutionary studies performed by members of the Porto Alegre group (2002-present).

Table 3 presents some selected examples of studies of general nature and of those involving microorganisms. Recently, Cazé et al. (2016)Cazé ALR, Mäder G, Nunes T, Queiroz LP, Oliveira G, Diniz Filho JAF, Bonatto SL and Freitas LB (2016) Could refuge theory and rivers acting as barriers explain the genetic variability distribution in the Atlantic Forest? Mol Phylogenet Evol 101:1-16. considered the question of factors affecting the genetic variability of the Atlantic Forest, with special reference to the refuge theory and river barriers.

Selected studies on plants are listed in Table 4. A large number of proteins of different types were surveyed in many species, searching for factors involved in their evolution. Specific studies in nine taxonomic families were indicated in the table, and specific mention can be made of a phylogenetic study with ecological niche modeling in the Myrtaceae (Turchetto-Zolet et al., 2016Turchetto-Zolet AC, Salgueiro F, Turchetto C, Cruz F, Veto NM, Barros MJF, Segatto ALA, Freitas LB and Margis R (2016) Phylogeography and ecological niche modeling in Myrtaceae suggest distinct vegetational responses to climate change between the southern and northern Atlantic Forest. Bot J Linn Soc 182:670-688.), relating them with climate changes in the southern and northern Atlantic Forest.

Animal research, in species ranging all the way from Platyhelminthes to primates, is mentioned in Table 5. The Paired box (PAX) family of transcription regulators and developmental genes plays a key role in numerous stages of embryonic development, and its variability from Porifera to Vertebrates was investigated by Paixão-Côrtes et al. (2015)Paixão-Côrtes VR, Salzano FM and Bortolini MC (2015) Origins and evolvability of the PAX family. Sem Cell Dev Biol 44:64-74.. At another level, an analysis of the Drosophilid fauna was performed to address the question of the conservation units in the Caating biome (Oliveira et al., 2016Oliveira FG, Garcia ACL, Montes MA, Juca JCL, Valente VLS and Rohde C (2016) Are conservation units in the Caatinga biome, Brazil, efficient in the protection of biodiversity? An analysis based on the drosophilid fauna. J Nat Conserv 34:145-150.).

Selected examples of human evolutionary studies are given in Table 6. The whole genomes of Homo sapiens, Homo neanderthalensis, and Denisovans were searched by Paixão-Côrtes et al. (2013)Paixão-Côrtes VR, Salzano FM and Bortolini MC (2013) Evolutionary history of chordate PAX genes: Dynamics of change in a complex gene family. PLoS One 8:e73560. to investigate the question of possible differences in cognitive ability between extinct and extant hominins. Results from 51 genes that affect this ability indicated similarity, with all the derived alleles being present in the three entities; while alternative models of human evolution were tested by Fagundes et al. (2007)Fagundes NJR, Ray N, Neuenchwander S, Beaumont M, Salzano FM, Bonatto SL and Excoffier L (2007) Statistical evaluation of alternative models of human evolution. Proc Natl Acad Sci U S A 104:17614-17619..

Latin American populations were extensively investigated during the period considered, and the question of interethnic admixture dynamics was addressed by Salzano and Sans (2014)Salzano FM and Sans M (2014) Interethnic admixture and the evolution of Latin American populations. Genet Mol Biol 37(Suppl 1):151-170..

As for Amerindians, the prehistoric peopling of the Americas was examined in detail, using craniofacial morphology and uniparental genetic markers (González-José et al., 2008González-José R, Bortolini MC, Santos FR and Bonatto SL (2008) The peopling of America: Craniofacial shape variation on a continental scale and its interpretation from an interdisciplinary view. Am J Phys Anthropol 137:175-187.). The French Guiana Amerindians were investigated using protein and DNA (autosome, mtDNA, Y-chromosomal) markers, and the fundamental question of the relationship between gene and culture was addressed in several publications, especially for the Xavante (Hünemeier et al., 2012Hünemeier T, Amorim CEG, Azevedo S, Contini V, Acuña-Alonso V, Rothhammer F, Dugoujon J-M, Mazières S, Barrantes R, Villareal-Molina MT, et al. (2012). Evolutionary responses to a constructed niche: Ancient Mesoamericans as a model of gene-culture coevolution. PLoS One 7:e38862.). These Amerindians were the subject of a whole book published by Coimbra Jr et al. (2002)Coimbra Jr CEA, Flowers NM, Salzano FM and Santos RV (2002) The Xavante in Transition. Health, Ecology, and Bioanthropology in Central Brazil. University of Michigan Press, Ann Arbor, 344 pp..

The Porto Alegre Biological Evolution Workshops (PABEWs)

In 2006 our group, together with some other colleagues, considered it appropriate to start a cycle of international workshops in which key aspects of the evolutionary process could be discussed, where working hypotheses could be formulated and research projects delineated to answer questions. The invited persons, both Brazilian and foreigners, needed to have a wide vision of the evolutionary processes, which should be considered from a historical-philosophical point of view using empirical data from plant, animals, and humans. The first Workshop occurred in November, 2007, followed by four others in 2009, 2011, 2013, and 2015, always in November. Their format was also always the same: one-hour conferences, all by worldwide renown scholars, would be followed by 10 minutes of comments given by two specialists, followed by participation from the audience. The discussion period was always equal to that of the conference. The number of participants could not be more than 120, and attendance was subjected to previous selection, to assure that only persons already involved in evolutionary studies would attend.

The Fifth PABEW was held from November 9 to 11, 2015, in the Auditorium of our Department. It included 13 non-Brazilian speakers from Argentina, French Guiana, USA (3), UK (2), Norway, Switzerland (2), France, Spain, and Australia. Among the Brazilian commenting researchers 11 were from universities other than UFRGS. The meeting, as the previous ones, was a success for interchange of ideas and results, which in some instances led to the formation of joint research projects.

Final message

As was emphasized at the beginning of this article, the process of formation of research groups is a slow one, and their maintenance is always in danger due to internal or external factors. These difficulties are especially notable in Third World countries, making the maintenance of our group for almost seven decades a remarkable event. It was, therefore, appropriate to review these accomplishments now, especially since Brazil is in a new period of economic difficulties, and there are generalized misunderstandings among our government officials about the importance of science. I finish this paper by expressing my hopes that this situation will be transitory, and that we and colleagues from other institutions will continue to contribute in a significant way to world knowledge.

Acknowledgments

Over all these years our group has received generous funding from Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), and Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul (FAPERGS).

References

  • Albuquerque CMR and Napp M (1981) Genetic variability at the esterase-6 locus in natural populations of Drosophila simulans in relation to environmental heterogeneity. Genetics 98:399-407.
  • Araújo AM (1976) The relationship between altitude and cyanogenesis in white clover (Trifolium repens L.). Heredity 37:291-293.
  • Bonatto SL and Salzano FM (1997a) A single and early migration for the peopling of the Americas supported by mitochondrial DNA sequence data. Proc Natl Acad Sci U S A 94:1866-1871.
  • Bonatto SL and Salzano FM (1997b) Diversity and age of the four major mtDNA haplogroups and their implications for the peopling of the New World. Am J Hum Genet 61:1413-1423.
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  • Associate Editor: Klaus Hartfelder

Publication Dates

  • Publication in this collection
    19 Mar 2018
  • Date of issue
    2018

History

  • Received
    23 Feb 2017
  • Accepted
    27 Feb 2017
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