論文

査読有り
1998年11月

AML1(-/-) embryos do not express certain hematopoiesis-related gene transcripts including those of the PU.1 gene

ONCOGENE
  • H Okada
  • T Watanabe
  • M Niki
  • H Takano
  • N Chiba
  • N Yanai
  • K Tani
  • H Hibino
  • S Asano
  • ML Mucenski
  • Y Ito
  • T Noda
  • M Satake
  • 全て表示

17
18
開始ページ
2287
終了ページ
2293
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1038/sj.onc.1202151
出版者・発行元
STOCKTON PRESS

The AML1 and PEBP2 beta/CBF beta genes encode the DNA-binding and non-binding subunits, respectively, of the heterodimeric transcription factor, PEBP2/CBF. Targeting each gene results in an almost identical phenotype, namely the complete lack of definitive hematopoiesis in the fetal liver on embryonic day 11.5 (E11.5). We examined and compared the expression levels of various hematopoiesis-related genes in wild type embryos and in embryos mutated for AML1 or PEBP2 beta/CBF beta. The RNAs were prepared from the yolk sacs of E9.5 embryos, from the aorta-gonad- mesonephros regions of E11.5 embryos and from the livers of E11.5 embryos and RT-PCR was performed to detect various gene transcripts. Transcripts were detected for most of the hematopoiesis-related genes that encode transcription factors, cytokines and cytokine receptors, even in tissues from homozygously targeted embryos. On the other hand, PU.1 transcripts were never detected in any tissue of AML1(-/-) or PEBP2 beta/CBF beta(-/-) embryos. In addition, transcripts for the Vav, flk-2/flt-3, M-CSF receptor, G-CSF receptor and c-Myb genes were not detected in certain tissues of the (-/-) embryos. The results suggest that the expression of a particular set of hematopoiesis-related genes is closely correlated with the PEBP2/CBF function.

リンク情報
DOI
https://doi.org/10.1038/sj.onc.1202151
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000076723300002&DestApp=WOS_CPL
ID情報
  • DOI : 10.1038/sj.onc.1202151
  • ISSN : 0950-9232
  • Web of Science ID : WOS:000076723300002

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