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mRNA abundance changes during flagellar regeneration in Chlamydomonas reinhardtii.

机译:reinhardtii衣藻鞭毛再生过程中的mRNA丰度变化。

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Flagellar amputation in Chlamydomonas reinhardtii induces the accumulation of a specific set of RNAs, many of which encode flagellar proteins. We prepared a cDNA clone bank from RNA isolated from cells undergoing flagellar regeneration. From this bank, we selected clones that contain RNA sequences that display several different patterns of abundance regulation. Based on quantitation of the relative amounts of labeled, cloned cDNAs hybridizing to dots of RNA on nitrocellulose filters, the cloned sequences were divided into five regulatory classes: class I RNAs remain at constant abundance during flagellar regeneration; classes II, III, and IV begin to increase in abundance within a few minutes after deflagellation, reach maximal abundance at successively later times during regeneration, and return to control cell levels within 2 to 3 h; and class V RNA abundance decreases during flagellar regeneration. Alpha- and beta-tubulin mRNAs are included in regulatory class IV. The abundance kinetics of alpha-tubulin mRNAs differ slightly from those of beta-tubulin mRNAs. The availability of these clones makes possible studies on the mechanisms controlling the abundance of a wide variety of different RNA species during flagellar regeneration in Chlamydomonas.
机译:莱茵衣藻的鞭毛截肢诱导了一组特定RNA的积累,其中许多RNA编码鞭毛蛋白。我们从分离自鞭毛再生细胞的RNA中制备了cDNA克隆库。从该库中,我们选择了包含RNA序列的克隆,这些RNA序列显示了几种不同的丰度调节模式。基于对与硝酸纤维素滤膜上的RNA点杂交的标记克隆cDNA的相对量的定量,将克隆序列分为五种调节类别:I类RNA在鞭毛再生过程中保持恒定的丰度; II级,III级和IV级在爆鞭后数分钟内开始增加丰度,在再生期间随后的后续时间达到最大丰度,并在2-3小时内恢复到对照细胞水平;鞭毛再生过程中V类RNA丰度降低。 α-和β-微管蛋白mRNAs包括在IV级监管中。 α-微管蛋白mRNA的丰度动力学与β-微管蛋白mRNA的丰度动力学略有不同。这些克隆的可用性使人们可能对控制衣藻鞭毛再生期间控制各种不同RNA种类丰度的机制进行研究。

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