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Differential alterations in metabolic pattern of the six major UsnRNAs during development

机译:发育过程中六种主要UsnRNA代谢模式的差异变化

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The uridylic acid rich nuclear RNAs (U1-U6 snRNAs) are involved mainly in the processing of pre-mRNA and pre-rRNA. So, any control of cell growth through pre-mRNA/pre-rRNA processing may have some regulation through altered UsnRNAs metabolism. With this idea, attempts have been made to see how the metabolism of the six major UsnRNAs' changed during the normal process of cellular proliferation associated with differentiation from pluripotent/totipotent stem cells of early embryonic stage to much more differentiated state of different cell/tissue lineages in different tissues/organs during the fetal and neonatal stages of growth. It has been seen that the levels of the six major UsnRNAs were high in day 8 embryo when the cells were mainly pluripotent/totipotent in nature, and during the progression of embryonic development the levels of these UsnRNAs gradually decreased (35-65%) up to the midgestational period (day 13) with some exception, when the organogenesis has already been started. However in the fetal life, the levels of these UsnRNAs were maximum or comparable around 18 ± 2 days of gestation in comparison to that in day 8 embryo when the kinetics of the maturational status of the different organs were quite high. But, the levels of these UsnRNAs' became low during day 21 of fetal life or in day 0 of birth (perturation period) in all the tissues/organs except high UsnRNAs' level in spleen. In the neonatal life, around 3 ± 1 days of birth these UsnRNAs' levels again became maximum in all the tissues/organs (except in thymus) followed by decrease up to 5/6 days, and to become steady with slight increase within one to two weeks, when the kinetics of the organ maturation reached to a steady state. In case of thymus, the levels of the U3-U6 snRNAs were high on day 0 of birth followed by decrease in their level on day 1/2 and then increased to become steady within 2-4 weeks; whereas the U1 and U2 snRNAs' levels were high on day 3 of birth and the subsequent changes were similar to that in other tissues/organs. Thus the different UsnRNAs' metabolism in the perturation period and in the early stages of neonatal life has indicated the differential cellular functions in these two stages of development. These alterations in the metabolism of these UsnRNAs might be due to the differential changes in the rate of synthesis of these UsnRNAs and/or with their differential turnover rate in the different stages of development. Also, the differential variations of these UsnRNAs' levels have been observed among the different tissues/organs at the respective stages of development indicating the differences in the UsnRNAs' metabolism among the different cell/tissue lineages. Thus, it can be concluded that the metabolism of these UsnRNAs were developmentally regulated with some cell/tissue lineage variations, which might have some role in the developmentally regulated cellular process of proliferation and differentiation, through altered RNA splicing and processing.
机译:富含尿酸的核RNA(U1-U6 snRNA)主要参与前mRNA和前rRNA的加工。因此,通过前mRNA /前rRNA加工来控制细胞生长的任何方法都可能通过改变UsnRNA的代谢而具有一定的调节作用。有了这个想法,已经尝试了观察六种主要UsnRNA的代谢在正常的细胞增殖过程中如何发生变化,这些过程与从胚胎早期的多能/全能干细胞分化为不同细胞/组织的分化程度更高的状态有关胎儿和新生儿生长阶段不同组织/器官中的血统。已经发现,在自然界中细胞主要是多能/全能的情况下,第8天胚胎中六种主要的UsnRNA的水平较高,并且在胚胎发育的过程中,这些UsnRNA的水平逐渐降低(35-65%)。进入妊娠中期(第13天),但器官发生已经开始。但是,在胎儿生命中,与不同器官成熟状态的动力学相当高的第8天胚胎相比,这些UsnRNA的水平在妊娠18±2天左右达到最大值或相当。但是,这些UsnRNA的水平在胎儿生命的第21天或出生的第0天(摄动期)在所有组织/器官中都变低,除了脾中UsnRNA的水平高。在新生儿生命中,大约在出生后3±1天,这些UsnRNA的水平在所有组织/器官(胸腺除外)中再次达到最大值,随后降低至5/6天,并在1至1天内逐渐增加并稳定下来。两周后,当器官成熟的动力学达到稳定状态时。如果是胸腺,U3-U6 snRNA的水平在出生的第0天较高,然后在第1/2天下降,然后在2-4周内保持稳定。而在出生的第3天,U1和U2 snRNA的水平较高,随后的变化与其他组织/器官的相似。因此,在新生儿生命的摄动期和早期,不同的UsnRNAs的新陈代谢表明在这两个发育阶段中细胞功能的差异。这些UsnRNA代谢中的这些变化可能是由于这些UsnRNA的合成速率的差异变化和/或它们在不同发育阶段的更新率差异引起的。同样,在各个发育阶段的不同组织/器官之间已观察到这些UsnRNAs水平的差异,表明在不同细胞/组织谱系中UsnRNAs代谢的差异。因此,可以得出结论,这些UsnRNA的代谢受到某些细胞/组织谱系变异的发育调控,这可能通过改变RNA剪接和加工过程在发育调控的细胞增殖和分化过程中发挥一定作用。

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