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The inhibition of Beclin1-dependent autophagy sensitizes PTC cells to ABT737-induced death. 抑制 Beclin1 依赖性自噬使 PTC 细胞对 ABT737 诱导的死亡敏感。
IF 2.1 4区 生物学 Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-03-04 eCollection Date: 2024-01-01 DOI: 10.1590/1678-4685-GMB-2022-0170
Ning Hu, Yanhua Tian, Yanmei Song, Leilei Zang

ABT737 is used as a specific BCL2 inhibitor, which can treat papillary thyroid carcinoma (PTC). However, the effect of ABT737 on PTC cell apoptosis is limited. Moreover, BCL2 inhibition causes the activation of Beclin1-dependent autophagy. Our study aimed to explore the effects of autophagy and Beclin1 on ABT737 efficacy in PTC. The experimental data showed that ABT737 synchronously enhanced autophagic activity and apoptosis level in PTC cells. ABT737 also promoted the dissociation of BCL2-Beclin1 and BCL2-Bax complexes. Autophagy inhibitors, Bafilomycin A1 and 3-MA, enhanced the inhibitory effect of ABT737 on the survival and function in PTC cells. Consistently, autophagy inhibition with Beclin1 pharmacological inhibitor (spautin-1) also enhanced the efficacy of ABT737. Additionally, ABT737 at low-dose promoted LC3 conversion in PTC cells, and did not affect PTC cell apoptosis and survival. However, The efficacy of low-dose of ABT737 in PTC cell apoptosis and survival was displayed with the addition of Bafilomycin A1, 3-MA or spautin-1. In conclusion, the limited role of ABT737 in PTC cell apoptosis is attributed to its promoting effect on Beclin1-dependent autophagy. Therefore, autophagy inhibition based on Beclin1 downregulation can enhance the sensitivity of PTC cells to ABT737-induced death.

ABT737是一种特异性BCL2抑制剂,可用于治疗甲状腺乳头状癌(PTC)。然而,ABT737对PTC细胞凋亡的影响有限。此外,BCL2抑制会激活依赖于Beclin1的自噬。我们的研究旨在探讨自噬和Beclin1对ABT737在PTC中疗效的影响。实验数据显示,ABT737能同步增强PTC细胞的自噬活性和凋亡水平。ABT737还能促进BCL2-Beclin1和BCL2-Bax复合物的解离。自噬抑制剂巴佛洛霉素 A1 和 3-MA 增强了 ABT737 对 PTC 细胞存活和功能的抑制作用。同样,用Beclin1药理抑制剂(spautin-1)抑制自噬也增强了ABT737的疗效。此外,低剂量的 ABT737 还能促进 PTC 细胞中 LC3 的转化,并且不影响 PTC 细胞的凋亡和存活。然而,添加巴佛洛霉素 A1、3-MA 或 spautin-1 后,低剂量 ABT737 对 PTC 细胞凋亡和存活的疗效就会显现出来。总之,ABT737 对 PTC 细胞凋亡的有限作用归因于其对依赖 Beclin1 的自噬的促进作用。因此,基于下调 Beclin1 的自噬抑制可提高 PTC 细胞对 ABT737 诱导的死亡的敏感性。
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引用次数: 0
Investigating the effects of Carpesii fructus extract on the liver transcriptome of olive flounder (Paralichthys olivaceus) as a potential antiparasitic agent. 作为一种潜在的抗寄生虫药物,研究栉水母提取物对橄榄鲽(Paralichthys olivaceus)肝脏转录组的影响。
IF 2.1 4区 生物学 Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-03-04 eCollection Date: 2024-01-01 DOI: 10.1590/1678-4685-GMB-2023-0146
Sang Yoon Lee, Hwa Jin Lee, Na Young Kim, Min Sun Kim

Olive flounder (Paralichthys olivaceus), a popular aquaculture species, is plagued by the disease scuticociliatosis caused by Miamiensis avidus, which has a high mortality rate and is typically treated with chemicals such as formalin and hydrogen peroxide. However, Carpesii fructus extract has shown potential as a natural therapeutic agent by reducing the motility of M. avidus. However, despite its potential importance, the effect of the extract on fish metabolism remains unknown. In this study, the effect of Carpesii fructus extract and formalin on fish metabolism was analysed by whole transcriptome analysis in the liver of P. olivaceus. A total of 37,796 transcripts were generated and differential expression genes (DEGs) were identified in the liver of P. olivaceus treated with Carpesii fructus extract or formalin. In addition, functional analysis of DEGs between treatment groups was presented using Gene Ontology. These results will be crucial for the study of scuticociliatosis in various fish species, including P. olivaceus, and for the development of therapeutic agents for other diseases.

橄榄鲽(Paralichthys olivaceus)是一种广受欢迎的水产养殖品种,它深受由Miamiensis avidus引起的鳞鳃炎疾病的困扰,这种疾病的死亡率很高,通常使用福尔马林和过氧化氢等化学品进行治疗。然而,Carpesii 果实提取物通过降低 M. avidus 的运动能力,显示出作为天然治疗剂的潜力。然而,尽管这种提取物具有潜在的重要性,但其对鱼类新陈代谢的影响仍然未知。本研究通过对橄榄鱼肝脏进行全转录组分析,分析了胭脂鱼果提取物和福尔马林对鱼类新陈代谢的影响。研究共生成了 37,796 个转录本,并鉴定了经桔梗提取物或福尔马林处理的橄榄鱼肝脏中的差异表达基因(DEGs)。此外,还利用基因本体论对不同处理组之间的 DEGs 进行了功能分析。这些结果对于研究包括橄榄鱼在内的各种鱼类的鳞屑纤毛虫病以及开发其他疾病的治疗药物至关重要。
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引用次数: 0
Transcriptome data-based screening of potential host of genetic transformation for a blue-hued Bougainvillea transgene. 基于转录组数据筛选蓝花九重葛转基因的潜在基因转化宿主。
IF 2.1 4区 生物学 Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-03-04 eCollection Date: 2024-01-01 DOI: 10.1590/1678-4685-GMB-2023-0099
Rong Sun, Shan Liu, Jia Long, Jinglei Gao, Yi Diao

Bougainvillea is a popular ornamental plant. Although Bougainvillea is abundant in germplasm resources, cultivars and flower colors, there is no rare blue colour varieties, due to the absence of delphinidin-based anthocyanins. This study analyzed the Bougainvillea leaf and bract transcriptome to select hosts of genetic transformation that would be suitable for the accumulation of delphinidin. A total of 36 gigabyte (GB) of raw data was obtained by transcriptome sequencing, with 4,058 significantly differentially expressed genes, including 1,854 upregulated and 2,204 downregulated genes. Annotation of these genes was performed using Gene Ontology and Kyoto Encyclopedia of Genes and Genomes databases. Through annotation, two CHS genes, one F3H gene, one DFR gene, and one F3'H gene involved in the delphinidin biosynthesis pathway were identified. The expression levels of these genes and total flavonoid content in the bracts of six Bougainvillea varieties were examined through quantitative real-time PCR and spectrophotometry, respectively. Through the comprehensive evaluation based on membership function method, the suitable host order for a blue-hued Bougainvillea transgene is Singapore White>Elizabeth Angus>Ratana Yellow>China Beauty>Orange King>Brilliant Variegata. Thus, Singapore White variety was the most appropriate transgene host for blue-hued Bougainvillea. The results of this study provide a reference for the directed breeding of blue-hued Bougainvillea.

九重葛是一种广受欢迎的观赏植物。虽然九重葛的种质资源、栽培品种和花色都很丰富,但由于缺乏基于蝶形花素的花青素,目前还没有罕见的蓝色品种。本研究分析了九重葛叶片和苞片的转录组,以选择适合积累鹅掌楸素的基因转化宿主。通过转录组测序共获得了 36 千兆字节(GB)的原始数据,其中有 4,058 个显著差异表达的基因,包括 1,854 个上调基因和 2,204 个下调基因。利用基因本体和京都基因组百科全书数据库对这些基因进行了注释。通过注释,确定了 2 个 CHS 基因、1 个 F3H 基因、1 个 DFR 基因和 1 个 F3'H 基因参与蝶苷生物合成途径。通过实时定量 PCR 和分光光度法分别检测了这些基因的表达水平和六个九重葛品种苞片中的总黄酮含量。通过基于成员函数法的综合评价,蓝花九重葛转基因的适宜宿主顺序为:新加坡白>伊丽莎白安格斯>拉塔纳黄>中国美人>橙王>艳丽变种。因此,新加坡白品种是蓝花九重葛最合适的转基因宿主。该研究结果为蓝花九重葛的定向培育提供了参考。
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引用次数: 0
Prostate tumor markers: diagnosis, prognosis and management. 前列腺肿瘤标志物:诊断、预后和管理。
IF 2.1 4区 生物学 Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-02-26 eCollection Date: 2024-01-01 DOI: 10.1590/1678-4685-GMB-2023-0136
Gabriela Kniphoff da Silva Lawisch, Geórgia Muccillo Dexheimer, Vanderlei Biolchi, Rafael Armando Seewald, José Artur Bogo Chies

Prostate cancer (PCA) is the second most common type of cancer in the world. Nevertheless, diagnosis is still based on nonspecific methods, or invasive methods which makes clinical decision and diagnosis difficult, generating risk of both underdiagnosis and overdiagnosis. Given the high prevalence, morbidity and mortality of PCA, new strategies are needed for its diagnosis. A review of the literature on available biomarkers for PCA was performed, using the following terms: prostate cancer AND marker OR biomarker. The search was carried out in Pubmed, Science Direct, Web of Science and Clinical Trial. A total of 35 articles were used, and PHI (Prostate Health Index) and the 4Kscore tests were identified as the best well-established serum markers. These tests are based on the evaluation of expression levels of several molecules. For analysis of urine samples, Progensa, ExoDXProstate, and Mi Prostate Score Urine Test are available. All these tests have the potential to help diagnosis, avoiding unnecessary biopsies, but they are used only in association with digital rectal examination and PSA level data. The search for biomarkers that can help in the diagnosis and therapeutic management of PCA is still in its initial phase, requiring more efforts for an effective clinical application.

前列腺癌(PCA)是全球第二大常见癌症。然而,目前的诊断仍以非特异性方法或侵入性方法为基础,这给临床决策和诊断带来了困难,并可能导致诊断不足和诊断过度。鉴于 PCA 的高发病率、高发病率和高死亡率,我们需要新的诊断策略。我们使用以下术语对现有 PCA 生物标志物的文献进行了综述:前列腺癌、标志物或生物标志物。搜索范围包括 Pubmed、Science Direct、Web of Science 和 Clinical Trial。共使用了 35 篇文章,PHI(前列腺健康指数)和 4Kscore 测试被确定为最佳的成熟血清标记物。这些检测基于对几种分子表达水平的评估。对于尿液样本的分析,有 Progensa、ExoDXProstate 和 Mi Prostate Score 尿液检测。所有这些检测方法都有可能帮助诊断,避免不必要的活组织检查,但它们只能与数字直肠检查和 PSA 水平数据结合使用。寻找有助于 PCA 诊断和治疗管理的生物标志物的工作仍处于起步阶段,需要付出更多努力才能实现有效的临床应用。
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引用次数: 0
The good, the bad and the ugly of transposable elements annotation tools. 转座元件注释工具的好坏和丑陋。
IF 1.7 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2024-02-19 eCollection Date: 2024-01-01 DOI: 10.1590/1678-4685-GMB-2023-0138
Elgion L S Loreto, Elverson S de Melo, Gabriel L Wallau, Tiago M F F Gomes

Transposable elements are repetitive and mobile DNA segments that can be found in virtually all organisms investigated to date. Their complex structure and variable nature are particularly challenging from the genomic annotation point of view. Many softwares have been developed to automate and facilitate TEs annotation at the genomic level, but they are highly heterogeneous regarding documentation, usability and methods. In this review, we revisited the existing software for TE genomic annotation, concentrating on the most often used ones, the methodologies they apply, and usability. Building on the state of the art of TE annotation software we propose best practices and highlight the strengths and weaknesses from the available solutions.

可转座元件是一种重复和可移动的 DNA 片段,几乎存在于迄今为止研究过的所有生物体中。从基因组注释的角度来看,其复杂的结构和多变的性质尤其具有挑战性。目前已开发出许多软件来自动注释基因组水平上的隐性基因,但这些软件在文档、可用性和方法方面存在很大差异。在这篇综述中,我们重新审视了现有的 TE 基因组注释软件,重点关注最常用的软件、它们采用的方法和可用性。基于 TE 注释软件的技术现状,我们提出了最佳实践,并强调了现有解决方案的优缺点。
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引用次数: 0
Reduced gene flow and bottleneck in the threatened giant armadillo (Priodontes maximus): implications for its conservation. 濒危巨型犰狳(Priodontes maximus)基因流动的减少和瓶颈:对其保护的影响。
IF 2.1 4区 生物学 Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-02-19 eCollection Date: 2024-01-01 DOI: 10.1590/1678-4685-GMB-2023-0252
Nayra T Rodrigues, Bruno H Saranholi, Alexandre R Inforzato, Leandro Silveira, Arnaud Leonard Jean Desbiez, Pedro M Galetti

The progressive fragmentation and loss of habitats represent the main threats for endangered species, causing genetic consequences that may have potential implications for a population's long-term persistence. Large mammals are the most affected species among vertebrates. The giant armadillo Priodontes maximus is a large South American mammal threatened species, showing nocturnal, solitary and fossorial behavior, occurring at low population densities, and its population dynamics are still poorly known. In this study, we carried out the first assessment of genetic variability and population genetic structure of the species, using a panel of 15 polymorphic microsatellites developed by high-throughput genome sequencing. The spatial Bayesian clustering, Fst and Dest results indicated the presence of two genetic clusters (K = 2) in the study area. These results suggest a reduction in gene flow between individuals inhabiting the Brazilian savanna (Cerrado) and the Pantanal wetlands, with the increased human-driven habitat modifications possibly contributing for this scenario. A bottleneck signal was detected in both populations, and a subpopulation structuring in the Cerrado may also be reflecting consequences of the extensive habitat modifications. Findings from this study provide important and useful information for the future maintenance of genetic diversity and long-term conservation of this flagship species.

栖息地的逐渐破碎化和丧失是濒危物种面临的主要威胁,造成的遗传后果可能会影响种群的长期生存。大型哺乳动物是脊椎动物中受影响最严重的物种。巨型犰狳(Priodontes maximus)是南美洲大型哺乳动物中的濒危物种,具有夜行性、独居性和穴居性,种群密度较低,其种群动态至今仍鲜为人知。在这项研究中,我们利用高通量基因组测序技术开发的 15 个多态性微卫星面板,首次对该物种的遗传变异性和种群遗传结构进行了评估。空间贝叶斯聚类、Fst和Dest结果表明,研究区域存在两个遗传聚类(K = 2)。这些结果表明,居住在巴西热带稀树草原(Cerrado)和潘塔纳尔(Pantanal)湿地的个体之间的基因流动有所减少,而人类对栖息地的改造可能是造成这种情况的原因之一。在这两个种群中都发现了瓶颈信号,Cerrado地区的亚种群结构也可能反映了广泛的栖息地改变所造成的后果。这项研究的结果为今后保持这一旗舰物种的遗传多样性和长期保护提供了重要而有用的信息。
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引用次数: 0
bHLH-regulated routes in anther development in rice and Arabidopsis. 水稻和拟南芥花药发育过程中的 bHLH 调控途径。
IF 2.1 4区 生物学 Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-02-19 eCollection Date: 2024-01-01 DOI: 10.1590/1678-4685-GMB-2023-0171
Francieli Ortolan, Thomaz Stumpf Trenz, Camila Luiza Delaix, Fernanda Lazzarotto, Marcia Margis-Pinheiro

Anther development is a complex process essential for plant reproduction and crop yields. In recent years, significant progress has been made in the identification and characterization of the bHLH transcription factor family involved in anther regulation in rice and Arabidopsis, two extensively studied model plants. Research on bHLH transcription factors has unveiled their crucial function in controlling tapetum development, pollen wall formation, and other anther-specific processes. By exploring deeper into regulatory mechanisms governing anther development and bHLH transcription factors, we can gain important insights into plant reproduction, thereby accelerating crop yield improvement and the development of new plant breeding strategies. This review provides an overview of the current knowledge on anther development in rice and Arabidopsis, emphasizing the critical roles played by bHLH transcription factors in this process. Recent advances in gene expression analysis and functional studies are highlighted, as they have significantly enhanced our understanding of the regulatory networks involved in anther development.

花药发育是一个复杂的过程,对植物繁殖和作物产量至关重要。近年来,对水稻和拟南芥这两种研究广泛的模式植物中参与花药调控的 bHLH 转录因子家族的鉴定和表征取得了重大进展。对 bHLH 转录因子的研究揭示了它们在控制叶柄发育、花粉壁形成和其他花药特异过程中的关键功能。通过深入探索花药发育和 bHLH 转录因子的调控机制,我们可以获得有关植物繁殖的重要见解,从而加快作物产量的提高和新植物育种策略的开发。本综述概述了目前有关水稻和拟南芥花药发育的知识,强调了 bHLH 转录因子在这一过程中发挥的关键作用。文章重点介绍了基因表达分析和功能研究的最新进展,因为这些研究大大提高了我们对花药发育调控网络的认识。
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引用次数: 0
Boosting life sciences research in Brazil: building a case for a local Drosophila stock center. 促进巴西的生命科学研究:建立当地果蝇种群中心。
IF 2.1 4区 生物学 Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-02-19 eCollection Date: 2024-01-01 DOI: 10.1590/1678-4685-GMB-2023-0202
Marcos T Oliveira, Lucas Anhezini, Helena M Araujo, Marcus F Oliveira, Carlos A Couto-Lima

Drosophila melanogaster is undoubtedly one of the most useful model organisms in biology. Initially used in solidifying the principles of heredity, and establishing the basic concepts of population genetics and of the synthetic theory of evolution, it can currently offer scientists much more: the possibility of investigating a plethora of cellular and biological mechanisms, from development and function of the immune system to animal neurogenesis, tumorigenesis and beyond. Extensive resources are available for the community of Drosophila researchers worldwide, including an ever-growing number of mutant, transgenic and genomically-edited lines currently carried by stock centers in North America, Europe and Asia. Here, we provide evidence for the importance of stock centers in sustaining the substantial increase in the output of Drosophila research worldwide in recent decades. We also discuss the challenges that Brazilian Drosophila scientists face to keep their research projects internationally competitive, and argue that difficulties in importing fly lines from international stock centers have significantly stalled the progression of all Drosophila research areas in the country. Establishing a local stock center might be the first step towards building a strong local Drosophila community that will likely contribute to all areas of life sciences research.

黑腹果蝇无疑是生物学中最有用的模式生物之一。它最初被用于巩固遗传学原理、建立群体遗传学和进化合成理论的基本概念,而现在它能为科学家提供更多的东西:研究从免疫系统的发育和功能到动物神经发生、肿瘤发生等大量细胞和生物机制的可能性。全世界的果蝇研究人员都可以获得广泛的资源,包括目前由北美、欧洲和亚洲的基因库中心提供的越来越多的突变株、转基因株和基因组编辑株。在这里,我们提供了证据,证明近几十年来种群中心在维持全球果蝇研究成果大幅增长方面的重要性。我们还讨论了巴西果蝇科学家在保持其研究项目的国际竞争力方面所面临的挑战,并认为从国际种群中心进口果蝇品系的困难极大地阻碍了巴西所有果蝇研究领域的发展。建立本地种群中心可能是建立强大的本地果蝇群体的第一步,这将为生命科学研究的所有领域做出贡献。
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引用次数: 0
An overview of actionable and potentially actionable TSC1 and TSC2 germline variants in an online Database. 在线数据库中可操作和潜在可操作的 TSC1 和 TSC2 基因变异概述。
IF 2.1 4区 生物学 Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-02-19 eCollection Date: 2024-01-01 DOI: 10.1590/1678-4685-GMB-2023-0132
Arthur Bandeira de Mello Garcia, Guilherme Danielski Viola, Bruno da Silveira Corrêa, Taís da Silveira Fischer, Maria Clara de Freitas Pinho, Grazielle Motta Rodrigues, Patricia Ashton-Prolla, Clévia Rosset

Tuberous Sclerosis Complex (TSC) is caused by loss of function germline variants in the TSC1 or TSC2 tumor suppressor genes. Genetic testing for the detection of pathogenic variants in either TSC1 or TSC2 was implemented as a diagnostic criterion for TSC. However, TSC molecular diagnosis can be challenging due to the absence of variant hotspots and the high number of variants described. This review aimed to perform an overview of TSC1/2 variants submitted in the ClinVar database. Variants of uncertain significance (VUS), missense and single nucleotide variants were the most frequent in clinical significance (37-40%), molecular consequence (37%-39%) and variation type (82%-83%) categories in ClinVar in TSC1 and TSC2 variants, respectively. Frameshift and nonsense VUS have potential for pathogenic reclassification if further functional and segregation studies were performed. Indeed, there were few functional assays deposited in the database and literature. In addition, we did not observe hotspots for variation and many variants presented conflicting submissions regarding clinical significance. This study underscored the importance of disseminating molecular diagnostic results in a public database to render the information largely accessible and promote accurate diagnosis. We encourage the performance of functional studies evaluating the pathogenicity of TSC1/2 variants.

结节性硬化综合症(TSC)是由 TSC1 或 TSC2 肿瘤抑制基因中的功能缺失种系变异引起的。检测 TSC1 或 TSC2 中致病变体的基因检测被作为 TSC 的诊断标准。然而,由于缺乏变异热点和描述的变异数量较多,TSC 分子诊断可能具有挑战性。本综述旨在对ClinVar数据库中提交的TSC1/2变异进行综述。在临床意义(37%-40%)、分子后果(37%-39%)和变异类型(82%-83%)类别中,不确定意义变异(VUS)、错义变异和单核苷酸变异分别是ClinVar中最常见的TSC1和TSC2变异。如果进一步开展功能和分离研究,帧移位和无义 VUS 有可能被重新分类为致病基因。事实上,数据库和文献中存入的功能测定很少。此外,我们没有观察到变异的热点,许多变异在临床意义方面提交的材料相互矛盾。这项研究强调了在公共数据库中发布分子诊断结果的重要性,以便让更多人了解信息并促进准确诊断。我们鼓励开展功能研究,评估 TSC1/2 变异的致病性。
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引用次数: 0
Shades of white: The Petunia long corolla tube clade evolutionary history. 白色的阴影矮牵牛长花冠筒支系的进化史。
IF 2.1 4区 生物学 Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-02-12 eCollection Date: 2024-01-01 DOI: 10.1590/1415-4757-GMB-2023-0279
Alice Backes, Caroline Turchetto, Geraldo Mäder, Ana Lúcia A Segatto, Sandro L Bonatto, Loreta B Freitas

Delimiting species is challenging in recently diverged species, and adaptive radiation is fundamental to understanding the evolutionary processes because it requires multiple ecological opportunities associated with adaptation to biotic and abiotic environments. The young Petunia genus (Solanaceae) is an excellent opportunity to study speciation because of its association with pollinators and unique microenvironments. This study evaluated the phylogenetic relationships among a Petunia clade species with different floral syndromes that inhabit several environments. We based our work on multiple individuals per lineage and employed nuclear and plastid phylogenetic markers and nuclear microsatellites. The phylogenetic tree revealed two main groups regarding the elevation of the distribution range, whereas microsatellites showed high polymorphism-sharing splitting lineages into three clusters. Isolation by distance, migration followed by new environment colonization, and shifts in floral syndrome were the motors for lineage differentiation, including infraspecific structuring, which suggests the need for taxonomic revision in the genus.

在新近分化的物种中划分物种具有挑战性,而适应性辐射是理解进化过程的基础,因为它需要与适应生物和非生物环境相关的多种生态机会。年轻的矮牵牛属(茄科)与传粉媒介和独特的微环境有关,因此是研究物种演化的绝佳机会。本研究评估了栖息在多种环境中具有不同花综合征的矮牵牛科物种之间的系统发育关系。我们的研究基于每个品系的多个个体,并采用了核和质体系统发育标记以及核微卫星。系统发生树显示,在分布范围的抬升方面有两个主要群体,而微卫星则显示出高度的多态性共享,将各系分为三个群。距离隔离、迁徙后的新环境定植以及花期综合征的变化是导致世系分化(包括种下结构分化)的动因,这表明有必要对该属进行分类学修订。
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引用次数: 0
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