Identification of erythroid-enriched gene expression in the mouse embryonic yolk sac using microdissected cells.
Identification of erythroid-enriched gene expression in the mouse embryonic yolk sac using microdissected cells.
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使用显微解剖细胞鉴定小鼠胚胎卵黄囊中富含红系的基因表达。
DOI:
10.1002/dvdy.21426
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发表时间:
2008
期刊:
影响因子:
--
通讯作者:
Lloyd,JoyceA
中科院分区:
文献类型:
--
作者:
Redmond,LatashaC;Dumur,CatherineI;Archer,KellieJ;Haar,JackL;Lloyd,JoyceA
Little is known about the genes that control the embryonic erythroid program. Laser capture microdissection was used to isolate primitive erythroid precursors and epithelial cells from frozen sections of the embryonic day 9.5 yolk sac. The RNA samples were amplified and labeled for hybridization to Affymetrix GeneChip Mouse Genome 430A 2.0 arrays. Ninety‐one genes are expressed significantly higher in erythroid than in epithelial cells. Ingenuity pathway analysis indicates that many of these erythroid‐enriched genes cluster in highly significant biological networks. One of these networks containsRBTN2/LMO2,SCL/TAL1, andEKLF/KLF1, three of the very few genes required for primitive erythropoiesis. Quantitative real‐time polymerase chain reaction was used to verify thatplatelet factor 4,reelin,thrombospondin‐1, andmuscleblind‐like 1mRNA is erythroid‐enriched. These genes have established roles in development or differentiation in other systems, and are, therefore, good candidates for regulating primitive erythropoiesis. These results provide a catalog of genes expressed during primitive erythropoiesis. Developmental Dynamics 237:436–446, 2008. © 2008 Wiley‐Liss, Inc.