Konermann Carolin, Kresse Alexandra, Beuter-Gunia Cornelia, Würthner Jan, Degrandi Daniel, Pfeffer Klaus, Beer Sandra
Institute of Medical Microbiology and Hospital Hygiene, Heinrich-Heine University, Duesseldorf, Germany.
DNA Cell Biol. 2007 Dec;26(12):847-51. doi: 10.1089/dna.2007.0637.
In a systematic approach to identify interferon-gamma (IFN-gamma)-regulated host effector molecules, we found several members of the 65 kDa guanylate-binding proteins (GBPs) highly upregulated. During extensive characterization of these guanosine triphosphatases (GTPases), we identified discrepancies between the cloned and published sequences of the murine GTPase mGBP4. Two splice variants of mGBP4 could be detected. One variant led to a premature stop codon after 312 bp. The second variant resulted in a transcript with a disrupted G2 domain and was deposited as mGBP4.1 to the GenBank. Interestingly, only mGBP4, not mGBP4.1 mRNA, was highly upregulated in mice after infection with Listeria monocytogenes.
在一种系统的方法中,为了鉴定γ干扰素(IFN-γ)调节的宿主效应分子,我们发现65 kDa鸟苷酸结合蛋白(GBP)的几个成员高度上调。在对这些鸟苷三磷酸酶(GTP酶)进行广泛表征的过程中,我们发现小鼠GTP酶mGBP4的克隆序列与已发表序列之间存在差异。可以检测到mGBP4的两种剪接变体。一种变体在312 bp后导致提前终止密码子。第二种变体产生了一个G2结构域被破坏的转录本,并作为mGBP4.1存入GenBank。有趣的是,在感染单核细胞增生李斯特菌后,小鼠中只有mGBP4,而不是mGBP4.1 mRNA高度上调。