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Variable amounts of DNA related to the size of chloroplasts III. Biochemical determinations of DNA amounts per organelle

机译:可变数量的DNA与叶绿体的大小有关。每个细胞器DNA含量的生化测定

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摘要

Plastid genomes (plastomes) are part of the integrated compartmentalised genetic system of photoautotrophic eukaryotes. They are highly redundant and generally dispersed in several regions (nucleoids) within organelles. DNA quantities and number of DNA-containing regions per plastid vary and are developmentally regulated in a way not yet understood. Reliable quantitative data describing these patterns are scarce. We present a protocol to isolate fractions of pure plastids with varying average sizes from leaflets (≤1 mm) and leaves of different developmental stages continuously up to maturity (25 cm) from Beta vulgaris L. (sugar beet) to determine DNA amounts per organelle. The approach is based on plastid purification from homogenates of moderately fixed tissue by differential and isopycnic gradient centrifugations and on application of two different DNA specific colorimetric reactions after removing potentially interfering compounds. The sensitive fluorochrome DAPI (4′,6-diamidino-2-phenylindole) was used to estimate numbers and emission intensity of nucleoids per plastid. The amounts determined ranged from 0.15 to 4.9 × 10−2 pg DNA for plastids of 1→8 μm average diameter, corresponding from approximately a dozen to 330 genome equivalents per organelle and on average four to seven copies per nucleoid. The ratio of plastiduclear DNA changed continuously during leaf development from as little as 0.4% to about 20% in fully developed leaves. On the other hand, mesophyll cells of mature leaves differing in ploidy (di-, tri- and tetraploid) appeared to maintain a relatively constant nuclear genome/plastome ratio, equivalent to about 1,700 copies per C-value.
机译:质体基因组(质体组)是光合自养真核生物整合区室遗传系统的一部分。它们是高度冗余的,通常分散在细胞器内的几个区域(核苷)中。每个质体的DNA数量和包含DNA的区域的数量各不相同,并且以未知的方式进行发育调控。缺乏描述这些模式的可靠定量数据。我们提出了一种协议,从小叶(≤1毫米)和不同发育阶段的叶中连续不断地分离纯质体的平均大小,直到甜菜(B型甜菜)的成熟期(25厘米),以确定每个细胞器的DNA量。该方法基于通过差异和等温梯度离心从中等程度固定的组织匀浆中质体纯化,以及在去除潜在干扰化合物后应用两种不同的DNA特异性比色反应。敏感的荧光染料DAPI(4',6-二mid基-2-苯基吲哚)用于估计每个质体中类核苷的数量和发射强度。对于平均直径1→8μm的质体,测定的数量范围为0.15至4.9×10 −2 pg DNA,对应于每个细胞器约12至330个基因组当量,平均每个细胞器4至7个拷贝核苷。在叶片发育过程中,质体/核DNA的比例从完全发育的叶片中的0.4%不断变化到约20%。另一方面,不同倍性(二倍体,三倍体和四倍体)的成熟叶片的叶肉细胞似乎保持相对恒定的核基因组/质体组比率,相当于每个C值约1,700份。

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