Waldbeser L S, Chen Q, Crosa J H
Department of Molecular Microbiology and Immunology L220, School of Medicine, Oregon Health Sciences University, Portland 97201-3098, USA.
Mol Microbiol. 1995 Aug;17(4):747-56. doi: 10.1111/j.1365-2958.1995.mmi_17040747.x.
We have recently identified an antisense RNA (RNA alpha) that regulates the expression of the fatA iron transport gene encoding the outer membrane receptor for the iron-anguibactin complex. In this work, we demonstrate that RNA alpha also inhibits the expression of fatB, which encodes a 35 kDa iron transport protein and has domains homologous to other periplasmic transport proteins. The expression of fatA and fatB is repressed under iron-rich conditions, in which RNA alpha is induced. RNA alpha is homologous to two-thirds of the coding region of fatB. By cloning RNA alpha coding sequences immediately downstream of a tet promoter, we were able to obtain constitutive expression of the antisense RNA. The cloned region contains approximately 83% of the 650 nucleotide RNA alpha and is complementary to only 51% of the fatB mRNA but is still capable of causing a repression of the expression of the fatB gene. Our results in this work demonstrate that RNA alpha probably affects the stability of the fatB-specific mRNA.
我们最近鉴定出一种反义RNA(RNAα),它可调节fatA铁转运基因的表达,该基因编码铁-鳗弧菌素复合物的外膜受体。在这项研究中,我们证明RNAα也抑制fatB的表达,fatB编码一种35 kDa的铁转运蛋白,并且具有与其他周质转运蛋白同源的结构域。在富含铁的条件下,fatA和fatB的表达受到抑制,此时RNAα被诱导表达。RNAα与fatB编码区的三分之二同源。通过将RNAα编码序列克隆到tet启动子的紧邻下游,我们能够获得反义RNA的组成型表达。克隆区域包含约650个核苷酸的RNAα的83%,并且仅与51%的fatB mRNA互补,但仍然能够导致fatB基因表达的抑制。我们在这项工作中的结果表明,RNAα可能影响fatB特异性mRNA的稳定性。