Higgs D C, Colbert J T
Department of Botany, Iowa State University, Ames 50011-1020.
Plant Cell. 1994 Jul;6(7):1007-19. doi: 10.1105/tpc.6.7.1007.
We have identified possible mechanisms for the degradation of oat phytochrome A (PHYA) mRNA. The majority of PHYA mRNA molecules appeared to be degraded prior to removal of the poly(A) tail, a pathway that differs from that reported for the degradation of other eukaryotic mRNAs. Polyadenylated PHYA mRNA contained a pattern of putative degradation products that is consistent with a 5'-->3' exoribonuclease, although the participation of a stochastic endoribonuclease cannot be excluded. The poly(A) tail of PHYA mRNA was heterogeneous in size and ranged from approximately 14 to 220 nucleotides. Early PHYA mRNA degradation events did not appear to involve site-specific endoribonucleases. Approximately 25% of the apparently full-length PHYA mRNA was poly(A) deficient. Oat H4 histone, beta-tubulin, and actin mRNA populations had lower amounts of apparently full-length mRNAs that were poly(A) deficient. Degradation of the poly(A)-deficient PHYA mRNA, a second pathway, appeared to be initiated by a 3'-->5' exoribonucleolytic removal of the poly(A) tail followed by both 5'-->3' and 3'-->5' exoribonuclease activities. Polysome-associated RNA contained putative PHYA mRNA degradation products and was a mixture of polyadenylated and deadenylated PHYA messages, suggesting that the two distinct degradation pathways are polysome associated.
我们已经确定了燕麦光敏色素A(PHYA)mRNA降解的可能机制。大多数PHYA mRNA分子似乎在去除多聚腺苷酸尾巴之前就被降解了,这一途径不同于报道的其他真核mRNA的降解途径。多聚腺苷酸化的PHYA mRNA含有一系列推定的降解产物,这与5'→3'外切核糖核酸酶的作用模式一致,尽管不能排除随机内切核糖核酸酶的参与。PHYA mRNA的多聚腺苷酸尾巴大小不一,长度约为14至220个核苷酸。早期的PHYA mRNA降解事件似乎不涉及位点特异性内切核糖核酸酶。大约25%的明显全长的PHYA mRNA缺乏多聚腺苷酸。燕麦H4组蛋白、β-微管蛋白和肌动蛋白mRNA群体中明显全长但缺乏多聚腺苷酸的mRNA含量较低。缺乏多聚腺苷酸的PHYA mRNA的降解是第二条途径,似乎是由3'→5'外切核糖核酸酶去除多聚腺苷酸尾巴开始的,随后是5'→3'和3'→5'外切核糖核酸酶的活性。多核糖体相关RNA含有推定的PHYA mRNA降解产物,是多聚腺苷酸化和去腺苷酸化的PHYA信息的混合物,这表明这两种不同的降解途径与多核糖体相关。