Wissenshaftskolleg zu Berlin, Berlin, Germany.
The Milner Centre for Evolution, University of Bath, Bath, Somerset, United Kingdom.
PLoS Biol. 2022 Jul 5;20(7):e3001671. doi: 10.1371/journal.pbio.3001671. eCollection 2022 Jul.
Many human embryos die in utero owing to an excess or deficit of chromosomes, a phenomenon known as aneuploidy; this is largely a consequence of nondisjunction during maternal meiosis I. Asymmetries of this division render it vulnerable to selfish centromeres that promote their own transmission, these being thought to somehow underpin aneuploidy. In this essay, I suggest that these vulnerabilities provide only half the solution to the enigma. In mammals, as in utero and postnatal provisioning is continuous, the costs of early death are mitigated. With such reproductive compensation, selection can favour a centromere because it induces lethal aneuploidy: if, when taken towards the polar body, it instead kills the embryo via aneuploidy, it gains. The model is consistent with the observation that reduced dosage of a murine drive suppressor induces aneuploidy and with the fact that high aneuploidy rates in vertebrates are seen exclusively in mammals. I propose further tests of this idea. The wastefulness of human reproduction may be a price we pay for nurturing our offspring.
许多人类胚胎在子宫内死亡是由于染色体过多或不足,这一现象被称为非整倍体;这主要是由于母体减数分裂 I 过程中的不分离造成的。这种分裂的不对称性使其容易受到自私的着丝粒的影响,这些着丝粒促进自身的传递,人们认为这些着丝粒在某种程度上是导致非整倍体的原因。在这篇文章中,我认为这些脆弱性只提供了解决这个谜团的一半方法。在哺乳动物中,由于子宫内和产后的供应是连续的,早期死亡的代价降低了。有了这种生殖补偿,选择可以偏爱一个着丝粒,因为它会导致致命的非整倍体:如果它在向极体移动时,通过非整倍体杀死胚胎,它就会获得优势。该模型与这样一个观察结果一致,即减少鼠驱动抑制剂的剂量会诱导非整倍体,而且在脊椎动物中,高非整倍体率仅见于哺乳动物。我建议进一步测试这个想法。人类生殖的浪费可能是我们养育后代所付出的代价。