Cavalier-Smith T
J Cell Sci. 1978 Dec;34:247-78. doi: 10.1242/jcs.34.1.247.
The 40,000-fold variation in eukaryote haploid DNA content is unrelated to organismic complexity or to the numbers of protein-coding genes. In eukaryote microorganisms, as well as in animals and plants, DNA content is strongly correlated with cell volume and nuclear volume, and with cell cycle length and minimum generation time. These correlations are simply explained by postulating that DNA has 2 major functions unrelated to its protein-coding capacity: (1) the control of cell volume by the number of replicon origins, and (2) the determination of nuclear volume by the overall bulk of the DNA: cell growth rates are determined by the cell volume and by the area of the nuclear envelope available for nucleocytoplasmic transport of RNA, which in turn depends on the nuclear volume and therefore on the DNA content. During evolution nuclear volume, and therefore DNA content, has to be adjusted to the cell volume to allow reasonable growth rates. The great diversity of cell volumes and growth rates, and therefore of DNA contents, among eukaryotes results from a varying balance in different species between r-selection, which favours small cells and rapid growth rates and therefore low DNA C-values, and K-selection which favours large cells and slow growth rates and therefore high DNA C-values. In multicellular organisms cell size needs to vary in different tissues: size differences between somatic cells result from polyteny, endopolyploidy, or the synthesis of nucleoskeletal RNA. Conflict between the need for large ova and small somatic cells explains why lampbrush chromosomes, nurse cells, chromatin diminution and chromosome elimination evolved. Similar evolutionary considerations clarify the nature of polygenes, the significance of the distribution of haploidy, diploidy and dikaryosis in life cycles and of double fertilization in angiosperms, and of heteroploidy despite DNA constancy in cultured cells, and other puzzles in eukaryote chromosome biology. Eukaryote DNA can be divided into genic DNA (G-DNA), which codes for proteins (or serves as recognition sites for proteins involved in transcription, replication and recombination), and nucleoskeletal DNA (S-DNA) which exists only because of its nucleoskeletal role in determining the nuclear volume (which it shares with G-DNA, and performs not only directly, but also indirectly by coding for nucleoskeletal RNA). Mechanistic and evolutionary implications of this are discussed.
真核生物单倍体DNA含量的40000倍差异与生物体的复杂性或蛋白质编码基因的数量无关。在真核微生物以及动物和植物中,DNA含量与细胞体积、核体积、细胞周期长度和最短世代时间密切相关。这些相关性可以通过假设DNA具有与其蛋白质编码能力无关的两个主要功能来简单解释:(1)通过复制子起始点的数量控制细胞体积;(2)通过DNA的总体积决定核体积:细胞生长速率由细胞体积和可用于RNA核质运输的核膜面积决定,而这又取决于核体积,进而取决于DNA含量。在进化过程中,核体积以及DNA含量必须根据细胞体积进行调整,以保证合理的生长速率。真核生物中细胞体积、生长速率以及DNA含量的巨大差异,是由于不同物种在r选择(有利于小细胞和快速生长速率,因此DNA C值较低)和K选择(有利于大细胞和缓慢生长速率,因此DNA C值较高)之间的平衡不同所致。在多细胞生物中,不同组织的细胞大小需要有所不同:体细胞之间的大小差异源于多线化、核内多倍体或核骨架RNA的合成。大卵子与小体细胞需求之间的冲突解释了灯刷染色体、滋养细胞、染色质消减和染色体消除的进化原因。类似的进化考量阐明了多基因的本质、单倍体、二倍体和双核体在生命周期中的分布意义以及被子植物双受精的意义,以及尽管培养细胞中的DNA恒定但存在异倍体的原因,还有真核生物染色体生物学中的其他谜题。真核生物DNA可分为基因DNA(G-DNA),它编码蛋白质(或作为参与转录、复制和重组的蛋白质的识别位点),以及核骨架DNA(S-DNA),它仅因其在决定核体积方面的核骨架作用而存在(它与G-DNA共同发挥这一作用,不仅直接发挥作用,还通过编码核骨架RNA间接发挥作用)。本文讨论了其机制和进化意义。