Vol. XXXII Issue 1
Article 1
DOI:
10.35407/bag.2021.32.01.01
ARTÍCULOS ORIGINALES
More than a century of
cytogenetic studies in Chilean plants: how much have we progressed?
Más de un siglo de estudios citogenéticos en
plantas Chilenas: ¿cuánto hemos progresado?
Jara Seguel P.1,2 *
Palma Rojas C.3
1 Departamento de Ciencias Biológicas y Químicas. Facultad de
Recursos Naturales, Universidad Católica de Temuco, Casilla 15-D, Temuco, Chile.
2 Núcleo de Estudios Ambientales, Facultad de Recursos Naturales, Universidad
Católica de Temuco, Casilla 15-D, Temuco, Chile.
3 Departamento de Biología, Facultad de Ciencias, Universidad de La
Serena, Casilla 599, La Serena, Chile.
* Corresponding author: P. Jara Seguel pjara@uct.cl
ORCID 0000-0002-9340-1780
ABSTRACT
An overview is provided on the cytogenetic of Chilean plants,
highlighting information gathered from more than a century of work carried out
by foreign and national researchers who have contributed to the study of native
species. We briefly present the progress made to date and also emphasize some
strategies that, in our opinion, could spur further advances in this second
century of cytogenetic studies in Chilean plants.
Key words: Cytogenetics, Cytogenomics, Chilean plants
RESUMEN
Se presenta una visión general de la
citogenética de plantas chilenas, destacando información recopilada durante más
de un siglo de trabajo realizado por investigadores nacionales y extranjeros
que han contribuido al estudio de las especies nativas. Presentamos brevemente
los progresos realizados hasta la fecha y también destacamos algunas
estrategias que, en nuestra opinión, podrían impulsar mayores avances en este
segundo siglo de estudios citogenéticos en plantas chilenas.
Palabras clave: Citogenética, Citogenómica, Plantas chilenas
Received: 04/27/2021
Accepted: 04/30/2021
INTRODUCTION
The cytogenetics of Chilean plants has had a fragmented development
along its history, especially in its beginnings. In the last decades, however,
it has made important contributions to the study of plant diversity,
incorporating classical quantitative karyotype analysis and more recently
modern cytogenomic methods. However, in the present, strategies to further
progress have not yet been discussed among Chilean cytogeneticists. The first
study on the cytogenetics of Chilean plants reported the chromosome number of Alstroemeria
chilensis Lem. (Syn. Alstroemeria ligtu L., Alstroemeriaceae), which
was published by Strasburger (1882) almost at the end of
the 19th century in the Archiv für Mikrobiologie und Anatomie in Germany. Later
on, at the beginning of the 20th century, more studies on the cytogenetics of
Chilean plants were published from 1929 onwards. Since then, relevant
contributions have been made by foreign cytogeneticists such as Whyte (1929), Sato (1938, 1943), Goodspeed (1940), Titov de Tschicshow (1954) and Esponda (1970), who described
chromosome number and morphology in species of several native genera (e.g., Alstroemeria,
Bomarea, Lapageria and in back then Hippeastrum). At
that same time, Sanz (1955, 1965, 1968, 1970), a
Chilean cytogeneticist, made pioneering contributions applying cytogenetic
methods to plants, focusing his work on native species of the genera Alstroemeria,
Calceolaria, and Leucocoryne, among others. In later decades, a
gradual increase in chromosome studies of four botanical divisions (Bryophyta,
Pteridophyta, Pinophyta, and Magnoliophyta) including terrestrial and aquatic
plants is observed, with major advances achieved since 2001 until now. Some
reviews have discussed aspects on this subject which can be consulted for more
details (Jara Seguel and
Urrutia, 2012; Jara Seguel and Urrutia Estrada, 2018). In this
article we briefly present the progress on cytogenetic studies of Chilean
plants made to date, and also suggest some strategies that, in our opinion,
could spur further advances in this second century of cytogenetic studies.
HOW MUCH HAVE WE
PROGRESSED?
At present, 122 publications on cytogenetics are available covering ca.
402 Chilean plant species (Jara Seguel and Urrutia
Estrada, 2020). This number of studied species is equivalent to
6.5% of the total flora, according to statistics published in floristic reviews
(ca. 6,103 land plant species; Villagrán, 2020). This percentage is
alarmingly low compared to other regions around the world, with percentages
ranging from 35.0% in Italy to 80.0% in New Zealand (Peruzzi et al.
2011). Unfortunately, in South America only Paraguay (with ca. 313
studied species; Jara Seguel and Urrutia, 2012) and Brazil (with ca. 699
species studied from the Cerrado Ecoregion; Roa and Telles,
2017) have estimations on the number of studied species, representing the
only comparison parameter that we have to evaluate progress. The above paucity
is coupled with scant funding for projects on this specific issue in Chile.
Since 2007 only two government projects (FONDECYT) and one with academic
funding were awarded to a research group of the Universidad de Concepción
(Baeza C., Negritto M.; Repositorio ANID 2021). Our group (Jara Seguel P.,
Palma Rojas C.) receives financing annually from the Núcleo de Estudios
Ambientales (project MECESUP UCT0804, 2011) of the Universidad Católica de
Temuco, but the resources are mainly earmarked for operational expenses.
According to the number of species cytogenetically studied so far for Chilean
plants, it is clear that in the initial century the progresses were few and intermittent
(Jara Seguel and Urrutia 2012), experiencing difficulties such as the shortage
of Chilean specialists, which led to a large part of the studies being carried
out by foreign cytogeneticists. Publications recorded for the last decade show
that two Chilean research groups (those mentioned above) maintain active
productivity on the subject by focusing on various families and studying
different cytogenetic features e.g., chromosome number, karyotype morphology,
C-values, C and Ag- NOR banding, as well as cytogenomic markers e.g., 5S/45S
rDNA localization through the application of fluorescent in situ hybridization
(Baeza and Schrader, 2005; Baeza et al., 2007; Cajas et al.,
2009; Jara Seguel et al., 2012; Chacón et al.,
2012). Many of these chromosome data have been used to envisage phylogenetic
and evolutionary hypotheses in some families (Chacón et al., 2012; Jara
Seguel et al., 2021) with some species included in cytoevolutionary
studies of global flora (Smarda et al.,
2014; Carta et al.,
2020). Plant taxonomy has also required cytogenetic support in the case of
some families (Jara Seguel and Urrutia, 2012). Cytogeography is another
incipient line of research in Chile which could be useful to understand
patterns of distribution of cytogenetic diversity along the latitudinal and
longitudinal gradients of the continent or in insular areas with different
geographic locations and geological origins (Stuessy and
Baeza, 2017; Jara Seguel et al., 2020; 2021). Applications
in conservation genetics can also be visualized as an interesting field of
study in the near future (Jara Seguel and Urrutia, 2012; Jara Seguel et al.,
2020).
WHAT CAN WE DO IN THE
FUTURE?
In this second century of cytogenetic studies in Chilean plants, much
remains to be done and the challenges for the small Chilean community of
cytogeneticists are great. According to the statistics ca. 93.5% of the
Chilean native species have yet to be studied. In our opinion various
strategies are required to make further progress, and we propose: i) the
training of new specialists at the graduate and undergraduate level who are
willing to address this discipline of genetics instead of other branches
perhaps with a molecular approach, although obviously one does not exclude the
other; ii) specialization may also be necessary for current researchers
specifically in the fields of modern cytogenomics (Eykelenboom and
Tanaka 2020) and cytoinformatics (e.g., chromEvol, Mayrose et al., 2010), thus making it
possible to increase the critical mass of highly specialized cytogeneticists;
iii) the structuring of research groups necessarily has to be planned to ensure
that they work in cooperation in order to streamline efforts and financial
resources, either prioritizing endemic species (ca. 45% of the Chilean
continental flora) or those with conservation problems (ca. 70
critically threatened species); iv) monetary resources could be raised from
companies (mining, forestry, agricultural), charitable trusts, philanthropists
and environmentalists, i.e. all those social groups that are linked to the
direct use of native plants or that cause effects on them. The future advances
in cytogenetic studies of Chilean plants require the contribution of various
actors such as government, academia, research centers and economic groups. In
this third millennium, in the middle of the post-genomic era, progress in
cytogenetic studies is highly necessary for Chilean plants, especially with the
advent of global climate change that is strongly affecting the flora and the
ecosystems. In this scenario of biodiversity threat, it is necessary to
understand evolutionary aspects of Chilean plants, allowing cytogenetics to
contribute fundamental knowledge that could be included in modern phylogenomic
studies (Posada, 2016), encompassing the
analysis of different genome compartments (e.g., nuclear, plastidial, and
mitochondrial).
ACKNOWLEDGEMENTS
We would like to express our thanks to Núcleo de Estudios Ambientales
(NEA), Dirección General de Investigación of the Universidad Católica de
Temuco, Chile.
BIBLIOGRAPHY
Baeza C., Schrader O. (2005) Comparative karyotype analysis in Haplopappus
Cass. and Grindelia Willd. (Asteraceae) by double FISH with rDNA
specific genes. Plant Syst. Evol. 251:161-172.
Baeza C., Schrader O., Budahn H. (2007) Characterization of
geographically isolated accessions in five Alstroemeria L. species
(Chile) using FISH of tamdely repeated DNA sequences and RAPD analysis. Plant Syst. Evol. 269:1-14.
Cajas D., Baeza C.,
Ruiz E., Negritto M. (2009) Análisis
citogenético en poblaciones de Alstroemeria hookeri Lodd. ssp. hookeri
(Alstroemeriaceae) en la Región del Bío-Bío, Chile. Gayana Bot. 66(2):117-126.
Carta A., Bedini G., Peruzzi L. (2020) A deep dive into the ancestral
chromosome number and genome size of flowering plants. New Phytol. 228:1097-1106.
Chacón J., Sousa A., Baeza C., Renner S. (2012) Ribosomal DNA
distribution and a genus-wide phylogeny reveal patterns of chromosomal
evolution in Alstroemeria (Alstroemeriaceae). Am. J. Bot. 99:1501-1512.
Eykelenboom J., Tanaka T. (2020) Zooming in on chromosome dynamics. Cell
Cycle 19(12):1422-1432.
Esponda P. (1970) Cytotaxonomy of two species of the genus Hippeastrum
(Amarillidaceae) Cytologia 35(3):431- 433.
Goodspeed T. (1940) Amaryllidaceae of the University of California
botanical expedition to the Andes. Herbertia 7:17- 31.
Jara Seguel P., Palma Rojas C., Contreras J., von Brand E. (2012) Chromosome
localisation of nucleolar organizer region in Rhodophiala bagnoldii (Herb.)
Traub (Asparagales: Amaryllidaceae) determined by silver nitrate staining. Gayana
Bot. 69(1): 201-203.
Jara Seguel P., Urrutia J. (2012) Cytogenetics of Chilean angiosperms:
advances and prospects. Rev. Chil. Hist. Nat. 85:1-12.
Jara Seguel P., Urrutia Estrada J. (2018) Chilean Plants Cytogenetic
Database: coverage, characters and usages. J. Basic Appl. Genet. 29:65-69.
Jara Seguel P., Urrutia Estrada J. (2020) Chilean Plants Cytogenetic
Database. http://www.chileanpcd.com/ (accessed April 2021).
Jara Seguel P., Urrutia Estrada J., Vallejos N., Andrade E., Jara M. (2020)
Chromosome number variation in part of the flora of protected wild areas in the
Araucania Region of southern Chile. J. Basic. Appl. Genet. 31:27-38.
Jara Seguel P., Jara Arancio P., Andrade E., Urrutia Estrada J., Palma
Rojas C., Araya Jaime C. (2021) Cytogenetics of wild species of the
Alstroemeriaceae family (Liliales). Plant Syst. Evol. 307:34.
https://doi.org/10.1007/s00606-021-01756-1.
Mayrose I., Barker M., Otto S. (2010) Probabilistic models of chromosome
number evolution and the inference of polyploidy. Syst. Biol. 59:132-144.
Peruzzi L., Dawson M., Bedini G. (2011) Chromosome number variation in
two antipodean floras. AoB Plants. doi:10.1093/aobpla/plr020.
Posada D. (2016) Phylogenomics for Systematic Biology. Syst. Biol. 65(3):353-356.
Proyecto MECESUP UCT0804 (2011) Fortalecimiento
de las capacidades científicas y del post-grado a través del desarrollo de
núcleos de investigación en las áreas prioritarias de la Universidad Católica
de Temuco. Dirección General de Investigación y Posgrado, Universidad Católica
de Temuco, Chile.
Repositorio ANID (2021) Agencia Nacional
de Investigación y Desarrollo, Chile. http://repositorio.conicyt.cl/handle/10533/108045/browse?authority=f0574ffe-3fed-4a87-b37c-1be07497d275&type=author.
(accessed April
2021)
Roa F., Telles M. (2017) The Cerrado (Brazil) plant cytogenetics
database. Comp. Cytogen. 11(2): 285-297.
Sanz C. (1955) Observaciones cromosomales en plantas chilenas (II parte).
Agricultura Técnica (currently Chil. J. Agric. Res.) 15(1):5-11.
Sanz C. (1965) Observaciones cromosomales en plantas chilenas (III
parte). Agricultura Técnica (currently Chil. J. Agric. Res.) 25 (3): 124-127.
Sanz C. (1968) Determinación cromosomal en Huilli, Leucocoryne
ixioides Lindl. Agricultura Técnica (currently Chil. J. Agric. Res.) 28(1):10.
Sanz C. (1970) Observaciones cromosomales en Lapiedra chilensis. Agricultura
Técnica (currently Chil. J. Agric. Res.) 30(1):110.
Sato D. (1938) Karyotype alteration and phylogeny. IV. Karyotypes in
Amaryllidaceae with special reference to satchromosomes. Cytologia 9:226-240.
Sato D. (1943) Karyotype alteration and phylogeny in Liliaceae and
allied families. J. Jap. Bot. 12:57-161.
Smarda P., Bures P., Horová L., Leitch I., Mucina L., Pacini E., Tichý L.,
Grulich V., Rotreklová O. (2014) Ecological and evolutionary significance of
genomic GC content diversity in monocots. PNAS 111(39):4096-4102.
Strasburger E. (1882) Über den Teilungsvorgang der Zellkerne und das
Vehaltnis der Kernteilung zur Zellteilung. Arch. Mikrobiol. Anat. 21:476-596.
Stuessy T., Baeza M. (2017) Chromosome numbers. In: Stuessy T., Crawford
D., López-Sepúlveda P., Baeza C., Ruiz E. (Eds.) Plants of oceanic islands.
Evolution, biogeography, and conservation of the flora of the Juan Fernández
(Robinson Crusoe) Archipelago. Cambridge University Press, London, pp. 165-187.
Titov de Tschicshow N. (1954) Estudios
citológicos en Lapageria rosea Ruiz et Pavon. Boletín de la Sociedad de
Biología de Concepción 29: 3-6.
Villagrán C. (2020) Historia biogeográfica de las briófitas de Chile. Gayana Bot. 77(2):73-114.
Whyte R. (1929) Chromosome studies. I. Relationships of the genera Alstroemeria
and Bomarea. New Phytol. 28:319-344.