Gene/Protein
Disease
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Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
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Enzyme
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Query: EC:2.7.11.25 (
MEKK1
)
1,856
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
In plants and less-advanced animal species, such asC.elegans, introduction of exogenous double-stranded RNA (dsRNA) into cells would trigger degradation of the mRNA with homologous sequence and interfere with the endogenous gene expression. It might represent an ancient anti-virus response which could prevent the mutation in the genome that was caused by virus infection or mobile DNA elements insertion. This phenomenon was named RNA interference, or RNAi. In this study, RNAi was used to investigate the function of
basonuclin
gene during oogenesis. Microinjection of dsRNA directed towards
basonuclin
into mouse germinal-vesicle-intact (GV) oocytes brought down the abundance of the cognate mRNA effectively in a time- and concentration-dependent manner. This reduction effect was sequence-specific and showed no negative effect on other non-homologous gene expression in oocytes, which indicated that dsRNA can recognize and cause the degradation of the transcriptional products of endogenous
basonuclin
gene in a sequence-specific manner. Immunofluorescence results showed that RNAi could reduce the concentration of
basonuclin
protein to some extent, but the effect was less efficient than the dsRNA targeting towards tPA and
cMos
which was also expressed in oocytes. This result might be due to the long half life of
basonuclin
protein in oocytes and the short reaction time which was posed by the limited life span of GV oocytes cultured in vitro. In summary, dsRNA could inhibit the expression of the cognate gene in oocytes at both mRNA and protein levels. The effect was similar to Knock-out technique which was based on homologous recombination. Furthermore, hair-pin-style dsRNA targeting
basonuclin
gene could be produced by transcription from a recombinant plasmid and worked efficiently to deplete the cognate mRNA in oocytes. This finding offered a new way to study the function of
basonuclin
in the early stage of oogenesis by infection of primordial oocytes with the plasmid expressing hairpin-style
basonuclin
dsRNA.
...
PMID:Effects of exogenous double-stranded RNA on the basonuclin gene expression in mouse oocytes. 1876 91