Timing and characteristics of nuclear events during conjugation and genomic exclusion in Paramecium multimicronucleatum.

IF 5.8 2区 生物学 Q1 MARINE & FRESHWATER BIOLOGY Marine Life Science & Technology Pub Date : 2022-08-01 DOI:10.1007/s42995-022-00137-y
Xue Zhang, Xiaoteng Lu, Yong Chi, Yaohan Jiang, Chundi Wang, Saleh A Al-Farraj, Adriana Vallesi, Feng Gao
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引用次数: 11

Abstract

Ciliated protists are ideal material for studying the origin and evolution of sex, because of their nuclear dimorphism (containing both germline micronucleus and somatic macronucleus in the same cytoplasm), special sexual processes (conjugation and autogamy), and high diversity of mating-type systems. However, the study of sexual process is limited to only a few species, due to the difficulties in inducing or observing conjugation. In the present study, we investigate the conjugation process in Paramecium multimicronucleatum: (1) of the three prezygotic divisions, all micronuclei undergo the first two divisions (meiosis I, II), while a variable number of nuclei undergo the third division (mitosis); (2) the synkaryon divides three times after fertilization, giving rise to eight products that differentiate into four macronuclear anlagen and four micronuclei; (3) cells restore the vegetative stage after two successive cell fissions during which the macronuclear anlagen are distributed into daughter cells without division, while micronuclei divide mitotically; (4) the parental macronucleus begins to fragment following the first meiotic division and finally degenerates completely; (5) the entire process takes about 110 h, of which about 85 h are required for macronuclear development. In addition, we describe for the first time the process of genomic exclusion occurring between amicronucleate and micronucleate cells of P. multimicronucleatum, during which the micronucleate cell contributes a pronucleus to the amicronucleate cell, resulting in both exconjugants being homozygotes. These results provide new insights into the diversity of sexual processes and lay an important cytological basis for future in-depth studies of mating systems in ciliates.

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多微核草履虫偶联和基因组排除过程中核事件的时间和特征。
纤毛原生生物是研究性别起源和进化的理想材料,因为它们的核二态性(在同一细胞质中含有种系微核和体细胞大核),特殊的性过程(结合和自交配),以及交配型系统的高度多样性。然而,由于诱导或观察交配的困难,对性过程的研究仅限于少数物种。在本研究中,我们研究了多微核草履虫的接合过程:(1)在三次合子前分裂中,所有的微核都经历了前两次分裂(减数分裂I, II),而可变数量的核则经历了第三次分裂(有丝分裂);(2)合核在受精后分裂3次,产生8个产物,分别分化为4个大核原和4个微核原;(3)细胞在连续两次分裂后恢复营养状态,其中大核原原不分裂分布到子细胞中,而微核进行有丝分裂;(4)亲本大核在第一次减数分裂后开始分裂,最终完全退化;(5)整个过程耗时约110 h,其中大核发育所需时间约85 h。此外,我们首次描述了多微核假体的微核细胞和微核细胞之间发生的基因组排斥过程,在此过程中,微核细胞向微核细胞提供一个原核,导致两个接合子都是纯合子。这些结果提供了对交配过程多样性的新认识,并为进一步深入研究纤毛虫交配系统奠定了重要的细胞学基础。
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来源期刊
Marine Life Science & Technology
Marine Life Science & Technology MARINE & FRESHWATER BIOLOGY-
CiteScore
9.60
自引率
10.50%
发文量
58
期刊介绍: Marine Life Science & Technology (MLST), established in 2019, is dedicated to publishing original research papers that unveil new discoveries and theories spanning a wide spectrum of life sciences and technologies. This includes fundamental biology, fisheries science and technology, medicinal bioresources, food science, biotechnology, ecology, and environmental biology, with a particular focus on marine habitats. The journal is committed to nurturing synergistic interactions among these diverse disciplines, striving to advance multidisciplinary approaches within the scientific field. It caters to a readership comprising biological scientists, aquaculture researchers, marine technologists, biological oceanographers, and ecologists.
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