Chang W T, Lauzon R J
Department of Microbiology, Immunology and Molecular Genetics, Albany Medical College, New York 12208.
Biol Bull. 1995 Feb-Mar;188(1):23-31. doi: 10.2307/1542064.
The blastogenic (asexual) cycle of the colonial ascidian Botryllus schlosseri (Tunicata, Ascidiaceae) concludes in a cyclical phase of programmed cell and zooid death called takeover, in which all asexually derived adults die synchronously by apoptosis. The characterization of developmentally regulated genes whose expression patterns are selectively modulated during this process could pave the way to understand how this model organism dies. However, isolation of biologically functional RNA in this and other colonial ascidians with conventional phenol/chloroform-based procedures is hampered by extensive contamination of RNA preparations by pigments. Upon cell lysis, pigments that normally reside within specialized cells in the mantle wall of the adult are released and tightly associate with nucleic acids. Here, we report on the usefulness of a single-step RNA isolation method in which acid guanidinium isothiocyanate is used as an extraction medium, followed by preparative cesium chloride ultracentrifugation. This procedure successfully isolated biologically active, high-purity total RNA (OD260/OD280 = 1.9-2.1) from Botryllus colonies during takeover, as well as other species of colonial ascidians (Diplosoma macdonaldii, Botrylloides diegense) irrespective of pigmentation. Northern blot analysis performed with a 32P-labeled tunicate actin probe detected two polyadenylated transcripts of 1.5 and 1.7 kilobases in length from both growth phase and takeover colonies. Two-dimensional protein gel assays from in vitro translated mRNA preparations further revealed that specific transcripts were up-regulated during takeover, while others were repressed or down-regulated. Growth phase and takeover-specific cDNA libraries were constructed from pooled poly(A)+ RNA with a complexity of 1.0 x 10(7) and 1.2 x 10(7) recombinants respectively per 100 ng of cDNA before amplification.(ABSTRACT TRUNCATED AT 250 WORDS)
群体海鞘博特氏拟菊海鞘(被囊动物亚门,菊海鞘科)的增殖(无性)周期以一个程序性细胞和游动孢子死亡的循环阶段告终,这个阶段称为接管,在此过程中,所有无性繁殖产生的成体通过凋亡同步死亡。对在这一过程中其表达模式受到选择性调控的发育调控基因进行表征,可能为理解这种模式生物的死亡方式铺平道路。然而,使用基于苯酚/氯仿的传统方法在这种及其他群体海鞘中分离具有生物学功能的RNA时,RNA制剂会受到色素的广泛污染,从而受到阻碍。细胞裂解后,通常存在于成体外套壁特殊细胞内的色素被释放出来,并与核酸紧密结合。在此,我们报告一种单步RNA分离方法的效用,该方法使用酸性异硫氰酸胍作为提取介质,随后进行氯化铯制备性超速离心。此程序成功地从接管期间的博特氏拟菊海鞘群体以及其他群体海鞘物种(麦克唐纳双体海鞘、迪氏拟菊海鞘)中分离出了具有生物活性的高纯度总RNA(OD260/OD280 = 1.9 - 2.1),无论其色素沉着情况如何。用32P标记的海鞘肌动蛋白探针进行的Northern印迹分析检测到,来自生长阶段和接管群体的两个长度分别为1.5和1.7千碱基的聚腺苷酸化转录本。对体外翻译的mRNA制剂进行的二维蛋白质凝胶分析进一步表明,特定转录本在接管期间上调,而其他转录本则被抑制或下调。从合并的聚腺苷酸加尾RNA构建了生长阶段和接管特异性的cDNA文库,在扩增前,每100 ng cDNA的文库复杂度分别为1.0×10^7和1.2×10^7个重组体。(摘要截短于250字)