Trifa Y, Lerbs-Mache S
Laboratoire de Génétique Moléculaire des Plantes, Université Joseph Fourier and Centre National de la Recherche Scientifique, Grenoble, France.
Mol Gen Genet. 2000 May;263(4):642-7. doi: 10.1007/s004380051212.
We have previously characterised the cDNA corresponding to the nucleus-encoded, plastid ribosomal protein L4 from spinach. The L4 protein belongs to the group of ribosomal proteins for which extra-ribosomal functions have been demonstrated in prokaryotes. In general, these functions are concerned with the expression of ribosomal components. In order to analyse whether the plastid L4 protein might also have (an) extra-ribosomal function(s) we have produced the plastid L4 protein as a thioredoxin fusion protein and analysed its role in both prokaryotic (E. coli) and plastid systems. We found that the plastid L4 protein can replace the E. coli L4 protein in the NusA-dependent attenuation control of the E. coli S10 operon by stabilising stalled transcription complexes in a NusA-dependent reaction. In plastids, the L4 protein inhibits transcription of the rrn operon. Our results thus suggest extra-ribosomal function(s) for the plastid L4 protein in the expression of ribosomal components.
我们之前已对菠菜中与细胞核编码的质体核糖体蛋白L4相对应的cDNA进行了表征。L4蛋白属于核糖体蛋白组,在原核生物中已证明该组蛋白具有核糖体之外的功能。一般来说,这些功能与核糖体组分的表达有关。为了分析质体L4蛋白是否也可能具有核糖体之外的功能,我们将质体L4蛋白作为硫氧还蛋白融合蛋白进行表达,并分析了其在原核生物(大肠杆菌)和质体系统中的作用。我们发现,质体L4蛋白可以在大肠杆菌S10操纵子的NusA依赖性衰减控制中取代大肠杆菌L4蛋白,通过在NusA依赖性反应中稳定停滞的转录复合物来实现。在质体中,L4蛋白抑制rrn操纵子的转录。因此,我们的结果表明质体L4蛋白在核糖体组分的表达中具有核糖体之外的功能。