Travis R L, Anderson J M, Key J L
Department of Botany, University of Georgia, Athens, Georgia 30602.
Plant Physiol. 1973 Dec;52(6):608-12. doi: 10.1104/pp.52.6.608.
The influence of incubation and auxin (2,4-D) on polyribosome level in soybean hypocotyl was studied.A marked drop in the relative level of polyribosomes in excised apical or meristematic tissue (0 to 5 millimeters below the cotyledons) occurred during incubation. The addition of auxin to the incubation medium did not affect polyribosome level. A similar decrease in polyribosome level occurred in excised elongating tissue (5 to 15 millimeters below cotyledons) during incubation. Auxin, however, caused a small but highly reproducible stabilization of polyribosomes in this tissue. There was a rapid, but small, auxin-independent increase in polyribosomes of basal or nongrowing hypocotyl (from 20 to 40 millimeters below cotyledons) during incubation, followed by a larger auxin-dependent increase in polyribosomes. While auxin is known to cause an increase in total ribosomes during incubation of the excised basal hypocotyl, the observed transformation from monoribosomes to polyribosomes was not dependent on new ribosome synthesis.Protein synthetic activity (poly U-directed phenylalanine incorporation) of the 80S monoribosomes at low Mg(2+) levels increased during incubation of the excised basal hypocotyl. The increase in ribosome activity was biphasic (an initial auxin-independent phase followed by an auxin-dependent increase in activity) correlating with the biphasic increase in polyribosomes. The enhanced activity of 80S monoribosomes was related, at least in part, to an increase in the level of peptidyl-tRNA associated with the ribosome population. Removal of peptidyl-tRNA from the ribosomes reversed the auxin effect.The hypothesis is advanced that the increase in polyribosomes in response to incubation and to auxin is preceded by and dependent upon the activation of 80S monoribosomes. This activation is in addition to a requirement for continued RNA synthesis, at least in part mRNA, for the transition from monoribosomes to polyribosomes.
研究了温育和生长素(2,4 - D)对大豆下胚轴多核糖体水平的影响。在温育过程中,切除的顶端或分生组织(子叶以下0至5毫米)中多核糖体的相对水平显著下降。向温育培养基中添加生长素并不影响多核糖体水平。在温育过程中,切除的伸长组织(子叶以下5至15毫米)中多核糖体水平也出现类似下降。然而,生长素使该组织中的多核糖体有小幅但高度可重复的稳定。在温育过程中,基部或不生长的下胚轴(子叶以下20至40毫米)的多核糖体有快速但小幅的、不依赖生长素的增加,随后是更大的依赖生长素的增加。虽然已知生长素在切除的基部下胚轴温育期间会导致总核糖体增加,但观察到的从单核糖体向多核糖体的转变并不依赖于新核糖体的合成。在低镁(2 +)水平下,切除的基部下胚轴温育期间,80S单核糖体的蛋白质合成活性(多聚尿苷酸指导的苯丙氨酸掺入)增加。核糖体活性的增加是双相的(最初是不依赖生长素的阶段,随后是依赖生长素的活性增加),与多核糖体的双相增加相关。80S单核糖体活性的增强至少部分与核糖体群体中肽基 - tRNA水平的增加有关。从核糖体上去除肽基 - tRNA可逆转生长素的作用。提出的假说是,响应温育和生长素而导致的多核糖体增加之前并依赖于80S单核糖体的激活。这种激活除了至少部分mRNA的持续RNA合成外,对于从单核糖体向多核糖体的转变也是必需的。