Ehresmann B, Backendorf C, Ehresmann C, Millon R, Ebel J P
Eur J Biochem. 1980 Feb;104(1):255-62. doi: 10.1111/j.1432-1033.1980.tb04423.x.
The effects of ultraviolet irradiation on Escherichia coli 30-S ribosomal subunits were studied. At the doses of radiation used in this work (0-4.5 x 10(5) quanta/30-S subunit), only protein S7 was found to be significantly crosslinked to the 16-S RNA. In conditions where 25% of the protein was covalently crosslinked, the ability of the irradiated 30-S subunits to reassociate with 50-S subunits and their activity in polyphenylalanine synthesis decreased strongly. Similar results were obtained by irradiation with a germicide lamp (254 nm) or with a monochromatic ultraviolet light at 248 nm. No additional proteins were crosslinked to the 16-S RNA by irradiating 30-S subunits depleted in protein S1 or 70-S ribosomes. The covalent complex of 16-S RNA and protein S7 was isolated and digested by T1 ribonuclease. The oligonucleotide remaining attached to the crosslinked protein was characterised as A-C-C-U-C-G [position 1261 - 1266, see the sequence published by Carbon et al. (1979) Eur. J. Biochem. 160, 399-410]. Analysis of this fragment suggests that protein S7 was linked to the cytosine at position 1265 in the RNA sequence.
研究了紫外线照射对大肠杆菌30-S核糖体亚基的影响。在本研究中使用的辐射剂量下(0-4.5×10⁵量子/30-S亚基),仅发现蛋白质S7与16-S RNA发生了显著交联。在25%的蛋白质发生共价交联的条件下,经照射的30-S亚基与50-S亚基重新结合的能力及其在聚苯丙氨酸合成中的活性大幅下降。用杀菌灯(254nm)或248nm的单色紫外线照射也得到了类似结果。对缺乏蛋白质S1的30-S亚基或70-S核糖体进行照射,没有其他蛋白质与16-S RNA交联。分离出16-S RNA与蛋白质S7的共价复合物,并用T1核糖核酸酶进行消化。仍与交联蛋白相连的寡核苷酸被鉴定为A-C-C-U-C-G [位置1261 - 1266,见Carbon等人(1979年)发表的序列,《欧洲生物化学杂志》160,399-410]。对该片段的分析表明,蛋白质S7与RNA序列中位置1265处的胞嘧啶相连。