Germline-related molecular phenotype in Metazoa: conservation and innovation highlighted by comparative transcriptomics.

IF 4.1 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Evodevo Pub Date : 2023-01-30 DOI:10.1186/s13227-022-00207-3
Giovanni Piccinini, Liliana Milani
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引用次数: 1

Abstract

Background: In Metazoa, the germline represents the cell lineage devoted to the transmission of genetic heredity across generations. Its functions intuitively evoke the crucial roles that it plays in organism development and species evolution, and its establishment is tightly tied to animal multicellularity itself. The molecular toolkit expressed in germ cells has a high degree of conservation between species, and it also shares many components with the molecular phenotype of some animal totipotent cell lineages, like planarian neoblasts and sponge archaeocytes. The present study stems from these observations and represents a transcriptome-wide comparative analysis between germline-related samples of 9 animal species (7 phyla), comprehending also totipotent lineages classically considered somatic.

Results: Differential expression analyses were performed for each species between germline-related and control somatic tissues. We then compared the different germline-related transcriptional profiles across the species without the need for an a priori set of genes. Through a phylostratigraphic analysis, we observed that the proportion of phylum- and Metazoa-specific genes among germline-related upregulated transcripts was lower than expected by chance for almost all species. Moreover, homologous genes related to proper DNA replication resulted the most common when comparing the considered species, while the regulation of transcription and post-transcriptional mechanisms appeared more variable, showing shared upregulated functions and domains, but very few homologous whole-length sequences.

Conclusions: Our wide-scale comparative analysis mostly confirmed previous molecular characterizations of specific germline-related lineages. Additionally, we observed a consistent signal throughout the whole data set, therefore comprehending both canonically defined germline samples (germ cells), and totipotent cell lineages classically considered somatic (neoblasts and archaeocytes). The phylostratigraphic analysis supported the less probable involvement of novel molecular factors in the germline-related transcriptional phenotype and highlighted the early origin of such cell programming and its conservation throughout evolution. Moreover, the fact that the mostly shared molecular factors were involved in DNA replication and repair suggests how fidelity in genetic material inheritance is a strong and conserved driver of germline-related molecular phenotype, while transcriptional and post-transcriptional regulations appear differently tuned among the lineages.

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后生动物的种系相关分子表型:比较转录组学强调的保护和创新。
背景:在后生动物中,生殖系代表了致力于基因遗传跨代传递的细胞系。它的功能直观地唤起了它在生物发育和物种进化中所起的关键作用,它的建立与动物多细胞性本身密切相关。生殖细胞中表达的分子工具箱在物种之间具有高度的保守性,并且它与一些动物全能细胞系的分子表型有许多共同的成分,如虫新生细胞和海绵古细胞。本研究源于这些观察结果,代表了9种动物(7门)种系相关样本的转录组范围比较分析,包括经典认为是体细胞的全能性谱系。结果:在种系相关体细胞组织和对照体细胞组织中对每个物种进行了差异表达分析。然后,我们比较了不同物种的生殖系相关转录谱,而不需要先验的一组基因。通过系统地层学分析,我们观察到,在几乎所有物种的种系相关上调转录本中,门特异性和后生动物特异性基因的比例低于偶然预期。此外,与适当的DNA复制相关的同源基因在考虑的物种中最常见,而转录和转录后机制的调控则更加多样化,表现出共享的上调功能和结构域,但同源全长序列很少。结论:我们的大规模比较分析大部分证实了先前特定种系相关谱系的分子特征。此外,我们在整个数据集中观察到一致的信号,因此既理解了常规定义的生殖系样本(生殖细胞),也理解了通常被认为是体细胞的全能细胞系(新生细胞和古细胞)。系统地层学分析支持了一种可能性较小的新分子因子参与生殖系相关转录表型,并强调了这种细胞编程的早期起源及其在进化过程中的保护。此外,大多数共享的分子因子参与DNA复制和修复这一事实表明,遗传物质遗传的保真度是种系相关分子表型的一个强大而保守的驱动因素,而转录和转录后调控在谱系中似乎有所不同。
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来源期刊
Evodevo
Evodevo EVOLUTIONARY BIOLOGY-DEVELOPMENTAL BIOLOGY
CiteScore
7.50
自引率
0.00%
发文量
18
审稿时长
>12 weeks
期刊介绍: EvoDevo publishes articles on a broad range of topics associated with the translation of genotype to phenotype in a phylogenetic context. Understanding the history of life, the evolution of novelty and the generation of form, whether through embryogenesis, budding, or regeneration are amongst the greatest challenges in biology. We support the understanding of these processes through the many complementary approaches that characterize the field of evo-devo. The focus of the journal is on research that promotes understanding of the pattern and process of morphological evolution. All articles that fulfill this aim will be welcome, in particular: evolution of pattern; formation comparative gene function/expression; life history evolution; homology and character evolution; comparative genomics; phylogenetics and palaeontology
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