Julian F. Quintero-Galvis

Dr. Julian F. Quintero-Galvis


Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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31 May 2016 in Scientific Reports
Verified
Journal Article
Open access
JEJuan Diego Gaitan Espitia
Juan Diego Gaitan Espitia
JQJulian F. Quintero-Galvis
Julian F. Quintero-Galvis
AMAndres Mesas
Andres Mesas
GDGuillermo D’elía
Guillermo D’elía
Marine blue mussels (Mytilus spp.) are widespread species that exhibit an antitropical distribution with five species occurring in the Northern Hemisphere (M. trossulus, M. edulis, M. galloprovincialis, M. californianus and M. coruscus) and three in the Southern Hemisphere (M. galloprovincialis, M. chilensis and M. platensis). Species limits in this group remain controversial, in particular for those forms that live in South America. Here we investigated structural characteristics of marine mussels mitogenomes, based on published F mtDNA sequences of Northern Hemisphere species and two newly sequenced South American genomes, one from the Atlantic M. platensis and another from the Pacific M. chilensis. These mitogenomes exhibited similar architecture to those of other genomes of Mytilus, including the presence of the Atp8 gene, which is missing in most of the other bivalves. Our evolutionary analysis of mitochondrial genes indicates that purifying selection is the predominant force shaping the evolution of the coding genes. Results of our phylogenetic analyses supported the monophyly of Pteriomorphia and fully resolved the phylogenetic relationships among its five orders. Finally, the low genetic divergence of specimens assigned to M. chilensis and M. platensis suggests that these South American marine mussels represent conspecific variants rather than distinct species.

19 April 2016 in Scientific Reports
Verified
Journal Article
Open access
PDF file
HHHanane Hadj-Moussa
Hanane Hadj-Moussa
JMJason A. Moggridge
Jason A. Moggridge
BLBryan E. Luu
Bryan E. Luu
JQJulian F. Quintero-Galvis
Julian F. Quintero-Galvis
JEJuan Diego Gaitan Espitia
Juan Diego Gaitan Espitia
Kenneth B StoreyKenneth B Storey
Kenneth B Storey
When faced with adverse environmental conditions, the marsupial Dromiciops gliroides uses either daily or seasonal torpor to support survival and is the only known hibernating mammal in South America. As the sole living representative of the ancient Order Microbiotheria, this species can provide crucial information about the evolutionary origins and biochemical mechanisms of hibernation. Hibernation is a complex energy-saving strategy that involves changes in gene expression that are elicited in part by microRNAs. To better elucidate the role of microRNAs in orchestrating hypometabolism, a modified stem-loop technique and quantitative PCR were used to characterize the relative expression levels of 85 microRNAs in liver and skeletal muscle of control and torpid D. gliroides. Thirty-nine microRNAs were differentially regulated during torpor; of these, 35 were downregulated in liver and 11 were differentially expressed in skeletal muscle. Bioinformatic analysis predicted that the downregulated liver microRNAs were associated with activation of MAPK, PI3K-Akt and mTOR pathways, suggesting their importance in facilitating marsupial torpor. In skeletal muscle, hibernation-responsive microRNAs were predicted to regulate focal adhesion, ErbB, and mTOR pathways, indicating a promotion of muscle maintenance mechanisms. These tissue-specific responses suggest that microRNAs regulate key molecular pathways that facilitate hibernation, thermoregulation, and prevention of muscle disuse atrophy.

21 September 2018 in Molecular Ecology
Verified
Journal Article
Closed access
PDF file
RNRoberto Nespolo
Roberto Nespolo
JEJuan Diego Gaitan Espitia
Juan Diego Gaitan Espitia
JQJulian F. Quintero-Galvis
Julian F. Quintero-Galvis
FFFernanda V. Fernandez
Fernanda V. Fernandez
ASAndrea X. Ximena Silva Silva
Andrea X. Ximena Silva Silva
FBFrancisco Bozinovic
Francisco Bozinovic

1 March 2022 in Ecology and Evolution
Verified
Journal Article
Open access
Francisco E. FontúrbelFrancisco E. Fontúrbel
Francisco E. Fontúrbel
LPLida M Franco Perez
Lida M Franco Perez
FBFrancisco Bozinovic
Francisco Bozinovic
JQJulian F. Quintero-Galvis
Julian F. Quintero-Galvis
CMCarlos Mejías
Carlos Mejías
RNRoberto Nespolo
Roberto Nespolo
The arboreal marsupial monito del monte (genus Dromiciops, with two recognized species) is a paradigmatic mammal. It is the sole living representative of the order Microbiotheria, the ancestor lineage of Australian marsupials. Also, this marsupial is the unique frugivorous mammal in the temperate rainforest, being the main seed disperser of several endemic plants of this ecosystem, thus acting as keystone species. Dromiciops is also one of the few hibernating mammals in South America, spending half of the year in a physiological dormancy where metabolism is reduced to 10% of normal levels. This capacity to reduce energy expenditure in winter contrasts with the enormous energy turnover rate they experience in spring and summer. The unique life history strategies of this living Microbiotheria, characterized by an alternation of life in the slow and fast lanes, putatively represent ancestral traits that permitted these cold‐adapted mammals to survive in this environment. Here, we describe the ecological role of this emblematic marsupial, summarizing the ecophysiology of hibernation and sociality, updated phylogeographic relationships, reproductive cycle, trophic relationships, mutualisms, conservation, and threats. This marsupial shows high densities, despite presenting slow reproductive rates, a paradox explained by the unique characteristics of its three‐dimensional habitat. We finally suggest immediate actions to protect these species that may be threatened in the near future due to habitat destruction and climate change.

14 January 2022 in Molecular Phylogenetics and Evolution
Verified
Journal Article
Closed access
JQJulian F. Quintero-Galvis
Julian F. Quintero-Galvis
PSPablo Saenz-Agudelo
Pablo Saenz-Agudelo
GAGuillermo C. Amico
Guillermo C. Amico
SVSoledad Vazquez
Soledad Vazquez
ASAaron B.A. Shafer
Aaron B.A. Shafer
RNRoberto Nespolo
Roberto Nespolo

10 May 2016 in Ecology and Evolution
Verified
Journal Article
Open access
RPRocío Paleo‐López
Rocío Paleo‐López
JQJulian F. Quintero-Galvis
Julian F. Quintero-Galvis
JSJaiber J. Solano‐Iguaran
Jaiber J. Solano‐Iguaran
ASAngela Sanchez-Salazar
Angela Sanchez-Salazar
JEJuan Diego Gaitan Espitia
Juan Diego Gaitan Espitia
RNRoberto Nespolo
Roberto Nespolo
When novel sources of ecological opportunity are available, physiological innovations can trigger adaptive radiations. This could be the case of yeasts (Saccharomycotina), in which an evolutionary novelty is represented by the capacity to exploit simple sugars from fruits (fermentation). During adaptive radiations, diversification and morphological evolution are predicted to slow‐down after early bursts of diversification. Here, we performed the first comparative phylogenetic analysis in yeasts, testing the “early burst” prediction on species diversification and also on traits of putative ecological relevance (cell‐size and fermentation versatility). We found that speciation rates are constant during the time‐range we considered (ca., 150 millions of years). Phylogenetic signal of both traits was significant (but lower for cell‐size), suggesting that lineages resemble each other in trait‐values. Disparity analysis suggested accelerated evolution (diversification in trait values above Brownian Motion expectations) in cell‐size. We also found a significant phylogenetic regression between cell‐size and fermentation versatility (R 2 = 0.10), which suggests correlated evolution between both traits. Overall, our results do not support the early burst prediction both in species and traits, but suggest a number of interesting evolutionary patterns, that warrant further exploration. For instance, we show that the Whole Genomic Duplication that affected a whole clade of yeasts, does not seems to have a statistically detectable phenotypic effect at our level of analysis. In this regard, further studies of fermentation under common‐garden conditions combined with comparative analyses are warranted.