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  • LKLF  (1)
  • human β globin  (1)
  • 1
    ISSN: 1573-9368
    Keywords: human β globin ; 3′ enhancer ; transgenic ; promoter
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Our interest in thecis-acting elements that promote the up-regulation of the β globin gene has led to a systematic deletion analysis of portions of the β globin gene in the context of the HS2 and γ globin gene using transgenic mice. In constructs that delete the 5′ region to only 265 bp, high-level erythroid-specific expression was observed. Further deletion to 122 bp, however, results in significantly reduced expression levels A substitution of a minilocus control region for the single HS2 site was also produced, resulting in increased β globin expression over that seen with the HS2 alone. These results are consistent with the presence of an enhancer-like element between −122 and −265. In addition, a construct in which the entire β globin gene promoter was replaced by a thymidine kinase promoter was tested. Interestingly, no expression was detected in these transgenic mice. This may indicate the requirement for an erythroid-specific promoter to drive this gene. Finally, the 3′ region of the β globin gene was deleted in order to examine the effect of a previously defined 3′ enhancer region. With deletion of this region, the expression of the human β globin gene in transgenic mice is unchanged relative to the parental constructs.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Transgenic research 7 (1998), S. 229-238 
    ISSN: 1573-9368
    Keywords: LKLF ; gene targeting ; embryonic lethality
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Lung Kruppel-like factor (LKLF) is a member of the Kruppel-like family of zinc finger transcription factors and is closely related to erythroid kruppel-like factor (EKLF), which is necessary for β-globin gene expression. While EKLF is expressed exclusively in erythroid cells, LKLF is expressed temporally during early embryonic development and predominantly in the adult mouse lung. To understand the role this novel transcription factor plays in development as well as tissue differentiation and function, animals lacking LKLF were produced using gene targeting technology. Mice lacking LKLF die in utero between day 11.5 and 13.5 of embryonic life and exhibit retarded growth, craniofacial abnormalities, abdominal bleeding and signs of anaemia. Although the yolk sac erythropoiesis is normal in mutant embryos, in vitro fetal liver cultures of these embryos fail to give rise to erythroid cells. Expression of other erythroid specific genes such as EKLF, GATA1 and ...
    Type of Medium: Electronic Resource
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