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1.
G3 (Bethesda) ; 9(11): 3791-3800, 2019 11 05.
Artículo en Inglés | MEDLINE | ID: mdl-31690598

RESUMEN

A variety of genetic techniques have been devised to determine cell lineage relationships during tissue development. Some of these systems monitor cell lineages spatially and/or temporally without regard to gene expression by the cells, whereas others correlate gene expression with the lineage under study. The GAL4 Technique for Real-time and Clonal Expression (G-TRACE) system allows for rapid, fluorescent protein-based visualization of both current and past GAL4 expression patterns and is therefore amenable to genome-wide expression-based lineage screens. Here we describe the results from such a screen, performed by undergraduate students of the University of California, Los Angeles (UCLA) Undergraduate Research Consortium for Functional Genomics (URCFG) and high school summer scholars as part of a discovery-based education program. The results of the screen, which reveal novel expression-based lineage patterns within the brain, the imaginal disc epithelia, and the hematopoietic lymph gland, have been compiled into the G-TRACE Expression Database (GED), an online resource for use by the Drosophila research community. The impact of this discovery-based research experience on student learning gains was assessed independently and shown to be greater than that of similar programs conducted elsewhere. Furthermore, students participating in the URCFG showed considerably higher STEM retention rates than UCLA STEM students that did not participate in the URCFG, as well as STEM students nationwide.


Asunto(s)
Linaje de la Célula , Drosophila/genética , Animales , Encéfalo , Ojo , Expresión Génica , Sistema Linfático , Investigación , Estudiantes , Universidades , Alas de Animales
2.
Genome Biol ; 19(1): 77, 2018 06 11.
Artículo en Inglés | MEDLINE | ID: mdl-29890997

RESUMEN

BACKGROUND: Pear (Pyrus) is a globally grown fruit, with thousands of cultivars in five domesticated species and dozens of wild species. However, little is known about the evolutionary history of these pear species and what has contributed to the distinct phenotypic traits between Asian pears and European pears. RESULTS: We report the genome resequencing of 113 pear accessions from worldwide collections, representing both cultivated and wild pear species. Based on 18,302,883 identified SNPs, we conduct phylogenetics, population structure, gene flow, and selective sweep analyses. Furthermore, we propose a model for the divergence, dissemination, and independent domestication of Asian and European pears in which pear, after originating in southwest China and then being disseminated throughout central Asia, has eventually spread to western Asia, and then on to Europe. We find evidence for rapid evolution and balancing selection for S-RNase genes that have contributed to the maintenance of self-incompatibility, thus promoting outcrossing and accounting for pear genome diversity across the Eurasian continent. In addition, separate selective sweep signatures between Asian pears and European pears, combined with co-localized QTLs and differentially expressed genes, underline distinct phenotypic fruit traits, including flesh texture, sugar, acidity, aroma, and stone cells. CONCLUSIONS: This study provides further clarification of the evolutionary history of pear along with independent domestication of Asian and European pears. Furthermore, it provides substantive and valuable genomic resources that will significantly advance pear improvement and molecular breeding efforts.


Asunto(s)
Pyrus/genética , China , Domesticación , Europa (Continente) , Evolución Molecular , Frutas/genética , Flujo Génico/genética , Genoma de Planta/genética , Humanos , Fenotipo , Filogenia , Polimorfismo de Nucleótido Simple/genética , Sitios de Carácter Cuantitativo/genética
3.
Am J Med ; 125(7 Suppl): S15-7, 2012 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-22735746

RESUMEN

Primary care physicians (PCPs) may lack a basic understanding of myelodysplastic syndromes (MDS). Two case studies, presented to 44 internal medicine residents and outpatient attending internists, highlighted a potential knowledge gap. A differential diagnosis of MDS was overlooked in a 72-year-old man with several comorbidities and a hemoglobin level of 9.2 g/dL (historical levels, 10.8 to 11.2 g/dL). Despite the acute change in hemoglobin levels, and the presence of comorbid lung and heart disease, there was no immediate recommendation from the PCPs for specialist referral. In contrast, in the second case study a 76-year-old man with a 6-month history of recurrent infections, fatigue, a hemoglobin level of 7.2 g/dL, and multilineage cytopenias typifying the clinical presentation of MDS did receive further attention and workup. With these cases as background, this article examines the potential reasons for the failure of many PCPs to identify MDS, and suggests steps to be taken to improve its diagnosis, early referral, and treatment.


Asunto(s)
Síndromes Mielodisplásicos/diagnóstico , Médicos de Atención Primaria , Anciano , Diagnóstico Diferencial , Hemoglobinas/análisis , Humanos , Masculino
4.
Science ; 327(5963): 328-31, 2010 Jan 15.
Artículo en Inglés | MEDLINE | ID: mdl-20075252

RESUMEN

Artemisinin is a plant natural product produced by Artemisia annua and the active ingredient in the most effective treatment for malaria. Efforts to eradicate malaria are increasing demand for an affordable, high-quality, robust supply of artemisinin. We performed deep sequencing on the transcriptome of A. annua to identify genes and markers for fast-track breeding. Extensive genetic variation enabled us to build a detailed genetic map with nine linkage groups. Replicated field trials resulted in a quantitative trait loci (QTL) map that accounts for a significant amount of the variation in key traits controlling artemisinin yield. Enrichment for positive QTLs in parents of new high-yielding hybrids confirms that the knowledge and tools to convert A. annua into a robust crop are now available.


Asunto(s)
Antimaláricos/metabolismo , Artemisia/genética , Artemisia/metabolismo , Artemisininas/metabolismo , Mapeo Cromosómico , Genes de Plantas , Sitios de Carácter Cuantitativo , Cruzamientos Genéticos , ADN Complementario , Perfilación de la Expresión Génica , Estudios de Asociación Genética , Humanos , Malaria/tratamiento farmacológico , Mutación , Fenotipo , Polimorfismo de Nucleótido Simple , Análisis de Secuencia de ADN
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