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1.
Rev Cient Odontol (Lima) ; 12(2): e198, 2024.
Artículo en Español | MEDLINE | ID: mdl-39119126

RESUMEN

One of the biggest controversies in current orthodontics is determining the appliance to use, since today patients seek better results in shorter times, in addition to putting aesthetics first. OBJECTIVE: compare the benefits and disadvantages that arise when using fixed orthodontic appliances and transparent aligners. MATERIALS AND METHODS: An investigation and compilation of specialized bibliographic information on the topic was carried out in scientific search engines such as PubMed, SciElo and Web of Science between the years 1991 to 2023, focused on research work related to the effects of the use of orthodontic appliances. fixed compared to clear aligners. RESULTS: The review was carried out based on 53 articles found that met the selection criteria. CONCLUSION: Fixed orthodontic appliances are better in complex cases, they are more precise and less likely to relapse; Transparent aligners are more aesthetic, hygiene is more affective and the bone density of the mandibular condyle decreases.

2.
Genet Mol Biol ; 46(1 Suppl 1): e20220002, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-37017705

RESUMEN

Effective strategies for disease control are crucial for sustaining world food production and ensuring food security for the population. Wheat blast, a disease caused by the pathogen Magnaporthe oryzae pathotype Triticum, has been a concern for cereal producers and researchers due to its aggressiveness and rapid expansion. To solve this problem, the development of resistant varieties with durable resistance is an effective, economical and sustainable way to control the disease. Conventional breeding can be aided by several molecular tools to facilitate the mining of many sources of resistance, such as R genes and QTLs. The identification of new sources of resistance, whether in the wheat crop or in other cereals are an opportunity for efficient wheat breeding through the application of different techniques. Since this disease is still poorly studied in wheat, knowledge of the rice Magnaporthe pathotype may be adapted to control wheat blast. Thus, genetic mapping, molecular markers, transgenic approaches, and genomic editing are valuable technologies to fight wheat blast. This review aimed to compile the biotechnological alternatives available to accelerate the development of improved cultivars for resistance to wheat blast.

3.
Plants (Basel) ; 11(8)2022 Apr 14.
Artículo en Inglés | MEDLINE | ID: mdl-35448797

RESUMEN

In the present work, we study the genetic control of reproductive traits under different heat stress conditions in two populations of inbred lines derived from crosses between two S. pimpinellifolium accessions and two tomato cultivars (E9×L5 and E6203×LA1589). The temperature increase affected the reproductive traits, especially at extremely high temperatures, where only a few lines were able to set fruits. Even though a relative modest number of QTLs was identified, two clusters of QTLs involved in the responses of reproductive traits to heat stress were detected in both populations on chromosomes 1 and 2. Interestingly, several epistatic interactions were detected in the E9×L5 population, which were classified into three classes based on the allelic interaction: dominant (one locus suppressed the allelic effects of a second locus), co-adaptive (the double-homozygous alleles from the same parent alleles showed a higher phenotypic value than the combination of homozygous alleles from alternative parents) and transgressive (the combination of double-homozygous alleles from different parents showed better performance than double-homozygous alleles from the same parents). These results reinforce the important role of non-additive genetic variance in the response to heat stress and the potential of the new allelic combinations that arise after wide crosses.

4.
Front Plant Sci ; 13: 1019311, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36926258

RESUMEN

The genus Vitis belongs to the Vitaceae family and is divided into two subgenera: Muscadinia and Vitis, the main difference between these subgenera being the number of chromosomes. There are many hypotheses about the origin of the genus, which have been formed with archaeological studies and lately with molecular analyses. Even though there is no consensus on the place of origin, these studies have shown that grapes have been used by man since ancient times, starting later on its domestication. Most studies point to the Near East and Greece as the beginning of domestication, current research suggests it took place in parallel in different sites, but in all cases Vitis vinifera (L.) subsp. sylvestris [Vitis vinifera (L.) subsp. sylvestris (Gmelin) Hagi] seems to be the species chosen by our ancestors to give rise to the now known Vitis vinifera (L.) subsp. vinifera [=sativa (Hegi)= caucasica (Vavilov)]. Its evolution and expansion into other territories followed the formation of new empires and their expansion, and this is where the historical importance of this crop lies. In this process, plants with hermaphrodite flowers were preferentially selected, with firmer, sweeter, larger fruits of different colors, thus favoring the selection of genes associated with these traits, also resulting in a change in seed morphology. Currently, genetic improvement programs have made use of wild species for the introgression of disease resistance genes and tolerance to diverse soil and climate environments. In addition, the mapping of genes of interest, both linked to agronomic and fruit quality traits, has allowed the use of molecular markers for assisted selection. Information on the domestication process and genetic resources help to understand the gene pool available for the development of cultivars that respond to producer and consumer requirements.

5.
Funct Integr Genomics ; 22(1): 35-53, 2022 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-34751851

RESUMEN

Microsatellites (SSRs) are tandem repeat sequences in eukaryote genomes, including plant cytoplasmic genomes. The mitochondrial genome (mtDNA) has been shown to vary in size, number, and distribution of SSRs among different plant groups. Thus, SSRs contribute with genomic diversity in mtDNAs. However, the abundance, distribution, and evolutionary significance of SSRs in mtDNA from a wide range of algae and plants have not been explored. In this study, the mtDNAs of 204 plant and algal species were investigated related to the presence of SSRs. The number of SSRs was positively correlated with genome size. Its distribution is dependent on plant and algal groups analyzed, although the cluster analysis indicates the conservation of some common motifs in algal and terrestrial plants that reflect common ancestry of groups. Many SSRs in coding and non-coding regions can be useful for molecular markers. Moreover, mitochondrial SSRs are highly abundant, representing an important source for natural or induced genetic variation, i.e., for biotechnological approaches that can modulate mtDNA gene regulation. Thus, this comparative study increases the understanding of the plant and algal SSR evolution and brings perspectives for further studies.


Asunto(s)
Genoma Mitocondrial , Genoma de Planta , Repeticiones de Microsatélite , Plantas , ADN Mitocondrial/genética , Plantas/genética
6.
Zoology (Jena) ; 150: 125980, 2022 02.
Artículo en Inglés | MEDLINE | ID: mdl-34861535

RESUMEN

Tissue changes during embryonic and postnatal development are critical for the success of physiological processes later in mammalian life. Dietary transition from milk to a variety of other food items is one of the factors inducing these changes in mammal species. Blood is utilized as food by only three species of vampire bats among all living mammals. Considering its high protein content, this unique diet is known to induce several metabolic changes, including fasting susceptibility. However, changes in the renal function to meet the excretory needs associated to the blood diet are unknown. Here we aimed at investigating morphological alterations in vampires' kidneys during embryonic and post-natal development in order to better understand the evolutionary adaptations allowing sanguivory. Common vampire bats (Desmodus rotundus) were captured and had their kidneys removed for histological, morphometrical and stereological analysis. Our results showed increased glomerular area and higher glomerular and uriniferous tubules volumetric densities in adults compared to developing bats. These results, together with a higher Renal Somatic Index and a thicker inner medulla also reported for adults, support renal hypertrophy due to increased renal function in blood-feeding vampires as compared to the earlier life stages. We also report a lower foot process density and its different arrange inside the glomerular capsule in adults, indicating an adaptation to a larger extracellular volume formed by increased glomerular filtration. Taken together, kidney morphological changes reported here for vampire bats may reflect in adults' adaptations to a monotrophic strategy.


Asunto(s)
Quirópteros , Adaptación Fisiológica , Animales , Evolución Biológica , Dieta , Riñón/fisiología
7.
IBRO Neurosci Rep ; 11: 137-143, 2021 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-34693396

RESUMEN

Familial Adenomatous Polyposis (FAP) is an autosomal dominant disorder caused by mutation of the APC gene presenting with numerous colorectal adenomatous polyps and a near 100% risk of colon cancer. Preliminary research findings from our group indicate that FAP patients experience significant deficits across many cognitive domains. In the current study, fMRI brain metrics in a FAP population and matched controls were used to further the mechanistic understanding of reported cognitive deficits. This research identified and characterized any possible differences in resting brain networks and associations between neural network changes and cognition from 34 participants (18 FAP patients, 16 healthy controls). Functional connectivity analysis was performed using FSL with independent component analysis (ICA) to identify functional networks. Significant differences between cases and controls were observed in 8 well-established resting state networks. With the addition of an aggregate cognitive measure as a covariate, these differences were virtually non-existent, indicating a strong correlation between cognition and brain activity at the network level. The data indicate robust and pervasive effects on functional neural network activity among FAP patients and these effects are likely involved in cognitive deficits associated with this disease.

8.
Zoology (Jena) ; 144: 125861, 2021 02.
Artículo en Inglés | MEDLINE | ID: mdl-33232886

RESUMEN

Bats have adapted to many different feeding habits, which are known to induce morphophysiological adaptations in several tissues, especially those particularly involved with absorption, metabolism and excretion. The common vampire bat (Desmodus rotundus) has a very unique diet (blood), which, among other challenges, seems to pose a risk to their kidneys, due to the increased nitrogen excretion imposed by their remarkably high protein meal. Fruit-eating bats (Artibeus lituratus) consume a high carbohydrate diet and may be taken as a suitable species for this dietary comparative study. Here we aimed at investigating the renal morphology and stereology, kidneys antioxidant capacity, and plasma antidiuretic hormone (ADH) concentrations in adult fruit-eating and vampire bats. Sixteen animals were captured and used in this study, being 8 adult males from each species. Our results showed higher morphological standards of glomerular area, volumetric density of glomeruli, and renal somatic index for vampire bats, as well as higher reactive species of oxygen (ROS) production, such as nitric oxide (NO), higher plasma iron reduction ability (FRAP), higher activity of the antioxidant enzyme glutathione-S-transferase (GST) and a higher malondialdehyde production (MDA) in vampires' kidneys, compared to the fruit-eating species. The activities of the antioxidant enzymes superoxide dismutase (SOD) and catalase (CAT) were higher in fruit-eating bats. Plasma ADH concentrations were not different between species. Taken together, the renal morphophysiology conditions presented by vampire bats might be associated with a high demand for nitrogenous products excretion imposed by protein and iron overload. These features may play an important role on preventing protein-overload nephropathy, allowing vampires to survive under such a unique diet.


Asunto(s)
Quirópteros/anatomía & histología , Quirópteros/clasificación , Conducta Alimentaria , Riñón/anatomía & histología , Riñón/fisiología , Adaptación Fisiológica , Animales , Sangre , Quirópteros/fisiología , Dieta/veterinaria , Frutas , Masculino
9.
Odontoestomatol ; 23(38)2021.
Artículo en Español | LILACS-Express | LILACS | ID: biblio-1386396

RESUMEN

Resumen Esta investigación se centró en revisar los artículos que evaluaron cefalométricamente la posición de hueso hioides, posición lingual y la dimensión de la vía aérea faríngea según maloclusión esquelética, a fin de determinar si existe una relación entre estas estructuras. Método: Se identificaron publicaciones en las bases de datos: PubMed, Biblioteca Virtual en Salud (BVS), Scielo y Scopus. Palabras clave: Hueso hioides, Lengua, Vía aérea, Maloclusión. Se realizó un cribado de los artículos por título, resumen y texto completo, escritos en los idiomas inglés y español. Resultados: Se encontraron 75 artículos; se eliminaron 30, por no tener una relación directa con el tema. Finalmente, se seleccionaron 45 artículos. Se concluye que aún no hay un consenso absoluto, sobre la relación existente entre: la posición del hueso hioides, la lengua y la dimensión de la vía aérea superior; según maloclusión esquelética.


Resumo Esta investigação centrou-se na revisão dos artigos que avaliaram cefalometricamente a posição do osso hióide, a posição linguística e a dimensão da via aérea faríngea de acordo com a maloclusão esquelética, a fim de determinar se existe uma relação entre estes estruturas. Método: As publicações foram identificadas nas seguintes bases de dados: PubMed, Biblioteca Virtual em Saúde (BVS), Scielo e Scopus. Palavras-chave: Osso hióide, Língua, Via aérea, Maloclusão. Os artigos foram analisados por título, resumo e texto completo, escritos em inglês e espanhol. Resultados: Foram encontrados 75 artigos, 30 foram eliminados porque não estavam directamente relacionados com o tema. Finalmente, foram seleccionados 45 artigos. Conclui-se que ainda não existe consenso absoluto sobre a relação entre: a posição do osso hióide, a língua e a dimensão da via aérea superior, de acordo com a maloclusão esquelética.


Abstract This study reviewed the articles that evaluated hyoid bone position, tongue position, and pharyngeal airway dimension according to skeletal malocclusion cephalometrically to determine a connection between these structures. Method: Publications were identified in the following databases: PubMed, Virtual Health Library (VHL), Scielo, and Scopus. Keywords: hyoid bone, tongue, airway, malocclusion. The articles were screened by title, abstract and full text, written in English and Spanish. Results: We found 75 articles; 30 were discarded because they lacked a direct connection with the topic. Finally, 45 articles were selected. There is still no general consensus on the relationship between the position of the hyoid bone, the tongue, and the dimension of the upper airway according to skeletal malocclusion.

10.
medRxiv ; 2020 Nov 04.
Artículo en Inglés | MEDLINE | ID: mdl-33173924

RESUMEN

Familial Adenomatous Polyposis (FAP) is an autosomal dominant disorder caused by mutation of the APC gene presenting with numerous colorectal adenomatous polyps and a near 100% risk of colon cancer. Preliminary research findings from our group indicate that FAP patients experience significant deficits across many cognitive domains. In the current study, fMRI brain metrics in a FAP population and matched controls were used to further the mechanistic understanding of reported cognitive deficits. This research identified and characterized any possible differences in resting brain networks and associations between neural network changes and cognition from 34 participants (18 FAP patients, 16 healthy controls). Functional connectivity analysis was performed using FSL with independent component analysis (ICA) to identify functional networks. Significant differences between cases and controls were observed in 8 well-established resting state networks. With the addition of an aggregate cognitive measure as a covariate, these differences were virtually non-existent, indicating a strong correlation between cognition and brain activity at the network level. The data indicate robust and pervasive effects on functional neural network activity among FAP patients and these effects are likely involved in cognitive deficits associated with this disease.

11.
Artículo en Inglés | MEDLINE | ID: mdl-32123549

RESUMEN

BACKGROUND: Familial adenomatous polyposis (FAP) is an autosomal dominant disorder caused by germline mutations in the APC gene. Patients with FAP have multiple extraintestinal manifestations that follow a genotype-phenotype pattern; however, few data exist characterizing their cognitive abilities. Given the role of the APC protein in development of the central nervous system, we hypothesized that patients with FAP would show differences in cognitive functioning compared to controls. METHODS: Matched case-control study designed to evaluate cognitive function using the Test of Nonverbal Intelligence-4, the Bateria III Woodcock-Munoz, and the Behavior Rating Inventory of Executive Functions-Adult. Twenty-six individuals with FAP (mean age = 34.2 ± 15.0 years) and 25 age-gender and educational level matched controls (mean age = 32.7 ± 13.8 years) were evaluated. RESULTS: FAP-cases had significantly lower IQ (p = 0.005). Across all tasks of the Batería III Woodcock-Muñoz, FAP-cases performed significantly lower than controls, with all of the summary scores falling in the bottom quartile compared to controls (p < 0.0001). Patients with FAP scored within the deficient range for Long-Term Retrieval and Cognitive Fluency. CONCLUSION: APC protein has an important role in neurocognitive function. The pervasive nature of the observed cognitive dysfunction suggests that loss or dysfunction of the APC protein impacts processes in cortical and subcortical brain regions. Additional studies examining larger ethnically diverse cohorts with FAP are warranted.

12.
Rev. cuba. estomatol ; 56(4): e2065, oct.-dez. 2019. tab, graf
Artículo en Español | LILACS | ID: biblio-1093250

RESUMEN

RESUMEN Introducción: La determinación del ángulo SN-Frankfort ha sido una constante utilizada por muchas décadas con un valor de 7°, sin embargo, son diversas las investigaciones que han refutado esta afirmación, debido a que los factores sociodemográficos influyen en la variación de este ángulo. Asimismo, la importancia de determinarlo es pieza clave para establecer un diagnóstico certero. Objetivo: Evaluar la variación del ángulo SN-Frankfort según el biotipo facial en pacientes. Métodos: Estudio descriptivo, transversal, retrospectivo y observacional. La muestra estuvo conformada por 225 radiografías cefalométricas laterales de pacientes entre 12 a 35 años que acudieron al Servicio de Ortodoncia del Hospital Hipólito Unanue durante los años 2014-2017. Se cumplieron los criterios de inclusión y la selección se realizó de forma probabilística por el método aleatorio simple. Para la evaluación de las radiografías cefalométricas se realizó el trazado manual. El biotipo facial se determinó mediante el índice de VERT y luego se obtuvo el ángulo SN-Frankfort. Se emplearon dos métodos estadísticos para la evaluación de la concordancia y reproducibilidad: El índice de Kappa para la evaluación del biotipo facial y el coeficiente de correlación interclase para la determinación del ángulo. Resultados: El promedio del ángulo SN-Frankfort en los pacientes con biotipo dolicofacial fue de 10,46 ± 3,02°, con biotipo mesofacial 10,12 ± 3,03° y con biotipo braquifacial 10,39 ± 3,48°. Los pacientes del sexo femenino presentaron una mayor angulación SN-Frankfort (10,69 ± 3,04) en comparación con los pacientes del sexo masculino (9,73 ± 3,23); p= 0,026. Conclusiones: Existe una variación en el ángulo SN-Frankfort según el tipo de biotipo facial, sin embargo, estas diferencias no fueron significativas. De modo contrario, se encontró que existe una significativa mayor angulación de ángulo SN-Frankfort en los pacientes del sexo femenino(AU)


ABSTRACT Introduction: Determination of the SN-Frankfort angle has been a constant used for many decades with a value of 7°. However, several studies have refuted that statement, based on the influence of sociodemographic factors on the variation of this angle. On the other hand, the importance of its determination is crucial to achieve an accurate diagnosis. Objective: Evaluate the variation of the SN-Frankfort angle according to the facial biotype of patients. Methods: A descriptive cross-sectional observational retrospective study was conducted. The sample was 225 lateral cephalometric radiographs of patients aged 12-35 years attending the Orthodontics Service of Hipólito Unanue Hospital in the period 2014-2017. Inclusion criteria were complied with, and selection was made by simple random probability sampling. Manual tracing was performed to evaluate the cephalometric radiographs. Facial biotype was determined by the VERT index, and the SN-Frankfort angle was then obtained. Two statistical methods were used for agreement and reproducibility evaluation: the Kappa index for evaluation of the facial biotype and the interclass correlation coefficient for determination of the angle. Results: Average SN-Frankfort angle was 10.46 ± 3.02° for the dolichofacial biotype, 10.12 ± 3.03° for the mesofacial biotype and 10.39 ± 3.48° for the brachifacial biotype. Female patients had greater SN-Frankfort angulation (10.69 ± 3.04) than male patients (9.73 ± 3.23); p= 0.026. Conclusions: Variation was found in the SN-Frankfort angle according to the facial biotype, but those differences were not significant. Significantly greater SN-Frankfort angulation was found among female patients(AU)


Asunto(s)
Humanos , Masculino , Femenino , Adolescente , Adulto , Cefalometría/métodos , Base del Cráneo , Epidemiología Descriptiva , Estudios Transversales , Estudios Retrospectivos , Estudio Observacional
13.
Front Plant Sci ; 10: 727, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-31263469

RESUMEN

Background: Fusarium Head Blight (FHB) is a worldwide devastating disease of bread wheat (Triticum aestivum L.). Genetic resistance is the most effective way to control FHB and many QTL related to this trait have been mapped on the wheat genetic map. This information, however, must be refined to be more efficiently used in breeding programs and for the advance of the basic research. The objective of the present study was to in-depth analyze the QTLome of FHB resistance in bread wheat, further integrating genetic, genomic, and transcriptomic data, aiming to find candidate genes. Methods: An exhaustive bibliographic review on 76 scientific papers was carried out collecting information about QTL related to FHB resistance mapped on bread wheat. A dense genetic consensus map with 572,862 loci was generated for QTL projection. Meta-analysis could be performed on 323 QTL. Candidate gene mining was carried out within the most refined loci, containing genes that were cross-validated with publicly available transcriptional expression data of wheat under Fusarium infection. Most highlighted genes were investigated for protein evidence. Results: A total of 556 QTL were found in the literature, distributed on all sub-genomes and chromosomes of wheat. Meta-analysis generated 65 meta-QTL, and this refinement allows one to find markers more tightly linked to these regions. Candidate gene mining within the most refined meta-QTL, meta-QTL 1/chr. 3B, harvested 324 genes and transcriptional data cross-validated 10 of these genes, as responsive to FHB. One is of these genes encodes a Glycosiltransferase and the other encodes for a Cytochrome P450, and these such proteins have already been verified as being responsible for FHB resistance, but the remaining eight genes still have to be further studied, as promising loci for breeding. Conclusions: The QTLome of FHB resistance in wheat was successfully assembled and a refinement in terms of number and length of loci was obtained. The integration of the QTLome with genomic and transcriptomic data has allowed for the discovery of promising candidate genes for use in breeding programs.

14.
BMC Res Notes ; 12(1): 361, 2019 Jun 25.
Artículo en Inglés | MEDLINE | ID: mdl-31238948

RESUMEN

OBJECTIVES: This study was conducted to establish a method for early, quick and cheap screening of iron excess tolerance in rice (Oryza sativa L.) cultivars. RESULTS: Based on the experiments, iron excess leads to reduction in shoot length (SL) and this can be a useful characteristic for adequate screening of tolerant genotypes. The sensitive genotypes Nipponbare and BR-IRGA 409 indicated higher accumulation of iron in their tissues while BRS-Agrisul and Epagri 108 also accumulated iron, but at lower concentrations. BR-IRGA 410 displayed an intermediate phenotype regarding iron accumulation. No changes in shoot Cu content can be observed when comparing treatments. On the other hand, an increase was seen for Zn and Mn when shoots are subjected to Fe2+ excess. Fe stress at a lower concentration than 7 mM increased Zn but decreased Mn contents in shoots of BR-IRGA 409. Strong positive correlations were found here for Fe × Zn (0.93); Fe × Mn (0.97) and Zn × Mn (0.92), probably due to the Fe-induced activation of bivalent cation transporters. Results show that genotypes scored as sensitive present higher concentration of Fe in shoots and this is an efficient method to characterize rice cultivars regarding iron response.


Asunto(s)
Adaptación Fisiológica/genética , Pruebas Genéticas , Hierro/toxicidad , Oryza/genética , Oryza/fisiología , Adaptación Fisiológica/efectos de los fármacos , Genotipo , Oryza/efectos de los fármacos , Hojas de la Planta/efectos de los fármacos , Hojas de la Planta/fisiología , Brotes de la Planta/efectos de los fármacos , Brotes de la Planta/fisiología
15.
Ethn Dis ; 29(Suppl 1): 135-144, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-30906162

RESUMEN

The Research Centers in Minority Institutions (RCMI) program was established by the US Congress to support the development of biomedical research infrastructure at minority-serving institutions granting doctoral degrees in the health professions or in a health-related science. RCMI institutions also conduct research on diseases that disproportionately affect racial and ethnic minorities (ie, African Americans/Blacks, American Indians and Alaska Natives, Hispanics, Native Hawaiians and Other Pacific Islanders), those of low socioeconomic status, and rural persons. Quantitative metrics, including the numbers of doctoral science degrees granted to underrepresented students, NIH peer-reviewed research funding, peer-reviewed publications, and numbers of racial and ethnic minorities participating in sponsored research, demonstrate that RCMI grantee institutions have made substantial progress toward the intent of the Congressional legislation, as well as the NIH/NIMHD-linked goals of addressing workforce diversity and health disparities. Despite this progress, nationally, many challenges remain, including persistent disparities in research and career development awards to minority investigators. The continuing underrepresentation of minority investigators in NIH-sponsored research across multiple disease areas is of concern, in the face of unrelenting national health inequities. With the collaborative network support by the RCMI Translational Research Network (RTRN), the RCMI community is uniquely positioned to address these challenges through its community engagement and strategic partnerships with non-RCMI institutions. Funding agencies can play an important role by incentivizing such collaborations, and incorporating metrics for research funding that address underrepresented populations, workforce diversity and health equity.


Asunto(s)
Investigación Conductal , Investigación Biomédica , Grupos Minoritarios , Salud de las Minorías , Investigación Biomédica Traslacional , Investigación Conductal/métodos , Investigación Conductal/organización & administración , Investigación Biomédica/métodos , Investigación Biomédica/organización & administración , Diversidad Cultural , Etnicidad/educación , Etnicidad/estadística & datos numéricos , Disparidades en el Estado de Salud , Humanos , Grupos Minoritarios/educación , Grupos Minoritarios/estadística & datos numéricos , Salud de las Minorías/educación , Salud de las Minorías/etnología , Investigadores , Apoyo a la Investigación como Asunto , Investigación Biomédica Traslacional/métodos , Investigación Biomédica Traslacional/organización & administración , Estados Unidos , Recursos Humanos
16.
J Appl Genet ; 60(1): 27-31, 2019 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-30353473

RESUMEN

Narrowing of genetic diversity and the quantitative nature of most agronomic traits is a challenge for rice breeding. Genome-wide association studies have a great potential to identify important variation in loci underlying quantitative and complex traits; however, before performing the analysis, it is important to assess parameters of the genotypic data and population under study, to improve the accuracy of the genotype-phenotype associations. The aim of this study was to access the genetic diversity, linkage disequilibrium, and population structure of a working panel of Brazilian and several introduced rice accessions, which are currently being phenotyped for a vast number of traits to undergo association mapping. Ninety-four accessions were genotyped with 7098 SNPs, and after filtering for higher call rates and removing rare variants, 93 accessions and 4973 high-quality SNPs remained for subsequent analyses and association studies. The overall mean of the polymorphic information content, heterozygosity, and gene diversity of the SNPs was comparable to other rice panels. The r2 measure of linkage disequilibrium decayed to 0.25 in approximately 150 kb, a slow decay, explained by the autogamous nature of rice and the small size of the panel. Regarding population structure, eight groups were formed according to Bayesian clustering. Principle components and neighbor-joining analyses were able to distinguish part of the groups formed, mainly regarding the sub-species indica and japonica. Our results demonstrate that the population and SNPs are of high quality for association mapping.


Asunto(s)
Genética de Población , Desequilibrio de Ligamiento , Oryza/genética , Polimorfismo de Nucleótido Simple , Brasil , Mapeo Cromosómico , Estudios de Asociación Genética , Fitomejoramiento
17.
P R Health Sci J ; 37(Spec Issue): S85-S92, 2018 12.
Artículo en Inglés | MEDLINE | ID: mdl-30576584

RESUMEN

OBJECTIVE: Guillain-Barré syndrome (GBS) is an uncommon autoimmune disorder that follows infection or vaccination, and increased incidence has been reported during Zika virus (ZIKV) transmission. During the 2016 ZIKV epidemic, the Puerto Rico Department of Health (PRDH) implemented the Enhanced GBS Surveillance System (EGBSSS). Here, we describe EGBSSS implementation and evaluate completeness, validity, and timeliness. METHODS: GBS cases were identified using passive surveillance and discharge diagnostic code for GBS. Completeness was evaluated by capture-recapture methods. Sensitivity and positive predictive value (PPV) for confirmed GBS cases were calculated for both case identification methods. Median time to completion of key time steps were compared by quarter (Q1-4) and hospital size. RESULTS: A total of 122 confirmed GBS cases with onset of neurologic illness in 2016 were identified. Capture-recapture methodology estimated that four confirmed GBS cases were missed by both identification methods. Identification of cases by diagnostic code had a higher sensitivity than passive surveillance (89% vs. 80%), but a lower PPV (60% vs. 72%). There was a significant decrease from Q1 to Q3 in median time from hospital admission to case reporting (11 days vs. 2 days, p = 0.032) and from Q2 to Q3 in median time from specimen receipt to arbovirus laboratory test reporting (35 days vs. 26 days, p = 0.004). CONCLUSION: EGBSSS provided complete, valid, and increasingly timely surveillance data, which guided public health action and supported healthcare providers during the ZIKV epidemic. This evaluation provides programmatic lessons for GBS surveillance and emergency response surveillance.


Asunto(s)
Síndrome de Guillain-Barré/epidemiología , Vigilancia de la Población/métodos , Salud Pública , Infección por el Virus Zika/epidemiología , Epidemias , Síndrome de Guillain-Barré/diagnóstico , Síndrome de Guillain-Barré/virología , Hospitalización/estadística & datos numéricos , Humanos , Incidencia , Valor Predictivo de las Pruebas , Puerto Rico/epidemiología , Sensibilidad y Especificidad , Factores de Tiempo
18.
BMC Plant Biol ; 18(1): 349, 2018 Dec 12.
Artículo en Inglés | MEDLINE | ID: mdl-30541427

RESUMEN

BACKGROUND: SUMOylation is an essential eukaryotic post-translation modification that, in plants, regulates numerous cellular processes, ranging from seed development to stress response. Using rice as a model crop plant, we searched for potential regulatory points that may influence the activity of the rice SUMOylation machinery genes. RESULTS: We analyzed the presence of putative cis-acting regulatory elements (CREs) within the promoter regions of the rice SUMOylation machinery genes and found CREs related to different cellular processes, including hormone signaling. We confirmed that the transcript levels of genes involved in target-SUMOylation, containing ABA- and GA-related CREs, are responsive to treatments with these hormones. Transcriptional analysis in Nipponbare (spp. japonica) and LC-93-4 (spp. indica), showed that the transcript levels of all studied genes are maintained in the two subspecies, under normal growth. OsSUMO3 is an exceptional case since it is expressed at low levels or is not detectable at all in LC-93-4 roots and shoots, respectively. We revealed post-transcriptional regulation by alternative splicing (AS) for all genes studied, except for SUMO coding genes, OsSIZ2, OsOTS3, and OsELS2. Some AS forms have the potential to alter protein domains and catalytic centers. We also performed the molecular and phenotypic characterization of T-DNA insertion lines of some of the genes under study. Knockouts of OsFUG1 and OsELS1 showed increased SUMOylation levels and non-overlapping phenotypes. The fug1 line showed a dwarf phenotype, and significant defects in fertility, seed weight, and panicle architecture, while the els1 line showed early flowering and decreased plant height. We suggest that OsELS1 is an ortholog of AtEsd4, which was also supported by our phylogenetic analysis. CONCLUSIONS: Overall, we provide a comprehensive analysis of the rice SUMOylation machinery and discuss possible effects of the regulation of these genes at the transcriptional and post-transcriptional level. We also contribute to the characterization of two rice SUMO proteases, OsELS1 and OsFUG1.


Asunto(s)
Regulación de la Expresión Génica de las Plantas , Oryza/metabolismo , Sumoilación , Regulación de la Expresión Génica de las Plantas/genética , Genes de Plantas/genética , Oryza/enzimología , Oryza/genética , Péptido Hidrolasas/metabolismo , Filogenia , Proteínas de Plantas/genética , Proteína SUMO-1/genética , Sumoilación/genética
20.
Genet Mol Biol ; 41(3): 533-544, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30235398

RESUMEN

WRKY transcription factors (TFs) are responsible for the regulation of genes responsive to many plant growth and developmental cues, as well as to biotic and abiotic stresses. The modulation of gene expression by WRKY proteins primarily occurs by DNA binding at specific cis-regulatory elements, the W-box elements, which are short sequences located in the promoter region of certain genes. In addition, their action can occur through interaction with other TFs and the cellular transcription machinery. The current genome sequences available reveal a relatively large number of WRKY genes, reaching hundreds of copies. Recently, functional genomics studies in model plants have enabled the identification of function and mechanism of action of several WRKY TFs in plants. This review addresses the more recent studies in plants regarding the function of WRKY TFs in both model and crop plants for coping with environmental challenges, including a wide variety of abiotic and biotic stresses.

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