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Transcriptomic analysis of early B-cell development in the chicken embryo.
Nuthalapati, Nikhil K; Evans, Jeffrey D; Taylor, Robert L; Branton, Scott L; Nanduri, Bindu; Pharr, Gregory T.
Afiliación
  • Nuthalapati NK; Department of Basic Sciences, College of Veterinary Medicine, Mississippi State University, Mississippi State MS 39762, Mississippi State.
  • Evans JD; USDA, Agricultural Research Service, Poultry Research Unit, PO Box 5367, Mississippi State University, Starkville, MS 39762-5367.
  • Taylor RL; Division of Animal and Nutritional Sciences, West Virginia University, Morgantown, WV 26506.
  • Branton SL; USDA, Agricultural Research Service, Poultry Research Unit, PO Box 5367, Mississippi State University, Starkville, MS 39762-5367.
  • Nanduri B; Department of Basic Sciences, College of Veterinary Medicine, Mississippi State University, Mississippi State MS 39762, Mississippi State.
  • Pharr GT; Department of Basic Sciences, College of Veterinary Medicine, Mississippi State University, Mississippi State MS 39762, Mississippi State.
Poult Sci ; 98(11): 5342-5354, 2019 Nov 01.
Article en En | MEDLINE | ID: mdl-31237340
The chicken bursa of Fabricius is a primary lymphoid tissue important for B-cell development. Our long-term goal is to understand the role of bursal microenvironment in an early B-cell differentiation event initiating repertoire development through immunoglobulin gene conversion in the chick embryo. We hypothesize that early bursal B-cell differentiation is guided by signals through cytokine receptors. Our theory is based on previous evidence for expression of the receptor tyrosine kinase superfamily members and interleukin receptors in unseparated populations of bursal B-cells and bursal tissue. Knowledge of the expressed genes that are responsible for B-cell differentiation is a prerequisite for understanding the bursal microenvironment's function. This project uses transcriptomic analysis to evaluate gene expression across early B-cell development. RNA-seq was performed with total RNA isolated from bursal B-cells at embryonic day (ED) 16 and ED 19 (n = 3). Approximately 90 million high-quality clean reads were obtained from the cDNA libraries. The analysis revealed differentially expressed genes involved in the Jak-STAT pathway, Wnt signaling pathway, MAPK signaling pathway, metabolic pathways including tyrosine metabolism, Toll-like receptor signaling pathway, and cell-adhesion molecules. The genes predicted to encode surface receptors, signal transduction proteins, and transcription factors identified in this study represent gene candidates for controlling B-cell development in response to differentiation factors in the bursal microenvironment.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfocitos B / Pollos / Transcriptoma Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Poult Sci Año: 2019 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Linfocitos B / Pollos / Transcriptoma Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Poult Sci Año: 2019 Tipo del documento: Article Pais de publicación: Reino Unido