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染色质免疫选择确定了一个TAL-1靶基因。

Chromatin immunoselection defines a TAL-1 target gene.

作者信息

Cohen-Kaminsky S, Maouche-Chrétien L, Vitelli L, Vinit M A, Blanchard I, Yamamoto M, Peschle C, Roméo P H

机构信息

INSERM, U474, Hématologie Moléculaire, Hôpital Henri Mondor, 51 avenue du Maréchal de Lattre de Tassigny, 94010 Créteil, France.

出版信息

EMBO J. 1998 Sep 1;17(17):5151-60. doi: 10.1093/emboj/17.17.5151.

Abstract

Despite the major functions of the basic helix-loop-helix transcription factor TAL-1 in hematopoiesis and T-cell leukemogenesis, no TAL-1 target gene has been identified. Using immunoprecipitation of genomic fragments bound to TAL-1 in the chromatin of murine erythro-leukemia (MEL) cells, we found that 10% of the immunoselected fragments contained a CAGATG or a CAGGTG E-box, followed by a GATA site. We studied one of these fragments containing two E-boxes, CAGATG and CAGGTC, followed by a GATA motif, and showed that TAL-1 binds to the CAGGTG E-box with an affinity modulated by the CAGATG or the GATA site, and that the CAGGTG-GATA motif exhibits positive transcriptional activity in MEL but not in HeLa cells. This immunoselected sequence is located within an intron of a new gene co-expressed with TAL-1 in endothelial and erythroid cells, but not expressed in fibroblasts or adult liver where no TAL-1 mRNA was detected. Finally, in vitro differentiation of embryonic stem cells towards the erythro/megakaryocytic pathways showed that the TAL-1 target gene expression followed TAL-1 and GATA-1 expression. These results establish that TAL-1 is likely to activate its target genes through a complex that binds an E-box-GATA motif and define the first gene regulated by TAL-1.

摘要

尽管碱性螺旋-环-螺旋转录因子TAL-1在造血作用和T细胞白血病发生过程中发挥着主要功能,但尚未鉴定出TAL-1的靶基因。通过对小鼠红白血病(MEL)细胞染色质中与TAL-1结合的基因组片段进行免疫沉淀,我们发现10%的免疫选择片段含有CAGATG或CAGGTG E盒,随后是一个GATA位点。我们研究了其中一个包含两个E盒(CAGATG和CAGGTC)及一个GATA基序的片段,结果表明TAL-1以一种受CAGATG或GATA位点调控的亲和力与CAGGTG E盒结合,并且CAGGTG-GATA基序在MEL细胞中表现出正向转录活性,而在HeLa细胞中则没有。这个免疫选择序列位于一个与TAL-1在内皮细胞和红细胞中共同表达的新基因的内含子内,但在未检测到TAL-1 mRNA的成纤维细胞或成年肝脏中不表达。最后,胚胎干细胞向红细胞/巨核细胞途径的体外分化显示,TAL-1靶基因的表达与TAL-1和GATA-1的表达一致。这些结果表明,TAL-1可能通过与E盒-GATA基序结合的复合物来激活其靶基因,并确定了第一个受TAL-1调控的基因。

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