Orias E
Department of Biological Sciences, University of California, Santa Barbara 93106.
Biosystems. 1991;25(1-2):67-73. doi: 10.1016/0303-2647(91)90013-b.
Karyorelict ciliates have near diploid somatic nuclei (macronuclei) incapable of division. If selective pressure favors nuclear division, how could such macronuclei have evolved? I propose that they initially evolved in the context of a diplophase stage that consisted entirely of a non-dividing trophont that was terminated by the induction of meiosis. The diploid macronucleus then differentiated, functioned and was destroyed in the absence of cell division. Such a life cycle would necessarily be heterophasic, i.e. with alternating haploid and diploid generations. I call these ancestors heterophasic ciliates. I further propose that the ability of this diploid trophont to undergo binary fission arose de novo. Ciliate binary fission would then be a derived characteristic, which possibly evolved indepedently in more than one heterophasic ciliate lineage. A progression of steps, leading to the reduction of the haplophase and the generation of the karyorelict life cycle, is proposed. The shared possession of nuclear dimorphism with non-dividing macronuclei, conjugation, and a putative heterophasic ancestry invites further investigation of the phylogenetic relationship between heterokaryotic foraminifera and karyorelict ciliates.
核残遗纤毛虫具有近乎二倍体的体细胞细胞核(大核),无法进行分裂。如果选择压力有利于核分裂,那么这样的大核是如何进化而来的呢?我提出它们最初是在二倍体阶段的背景下进化而来的,这个阶段完全由一个不进行分裂的营养体组成,通过减数分裂的诱导而终止。然后,二倍体大核在没有细胞分裂的情况下进行分化、发挥功能并被破坏。这样的生命周期必然是异相的,即具有单倍体和二倍体世代交替。我将这些祖先称为异相纤毛虫。我进一步提出,这种二倍体营养体进行二分裂的能力是重新出现的。纤毛虫的二分裂将是一种衍生特征,可能在不止一个异相纤毛虫谱系中独立进化。本文提出了一系列步骤,导致单倍体阶段的减少和核残遗生命周期的产生。与不分裂的大核、接合以及假定的异相祖先共同拥有核二态性,这促使我们进一步研究异核有孔虫和核残遗纤毛虫之间的系统发育关系。