Physical shearing imparts biological activity to DNA and ability to transmit itself horizontally across species and kingdom boundaries

IF 2.946 Q3 Biochemistry, Genetics and Molecular Biology BMC Molecular Biology Pub Date : 2017-08-09 DOI:10.1186/s12867-017-0098-8
Gorantla Venkata Raghuram, Deepika Gupta, Siddharth Subramaniam, Ashwini Gaikwad, Naveen Kumar Khare, Malcolm Nobre, Naveen Kumar Nair, Indraneel Mittra
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引用次数: 11

Abstract

We have recently reported that cell-free DNA (cfDNA) fragments derived from dying cells that circulate in blood are biologically active molecules and can readily enter into healthy cells to activate DNA damage and apoptotic responses in the recipients. However, DNA is not conventionally known to spontaneously enter into cells or to have any intrinsic biological activity. We hypothesized that cellular entry and acquisition of biological properties are functions of the size of DNA.

To test this hypothesis, we generated small DNA fragments by sonicating high molecular weight DNA (HMW DNA) to mimic circulating cfDNA. Sonication of HMW DNA isolated from cancerous and non-cancerous human cells, bacteria and plant generated fragments 300–3000?bp in size which are similar to that reported for circulating cfDNA. We show here that while HMW DNAs were incapable of entering into cells, sonicated DNA (sDNA) from different sources could do so indiscriminately without heed to species or kingdom boundaries. Thus, sDNA from human cells and those from bacteria and plant could enter into nuclei of mouse cells and sDNA from human, bacterial and plant sources could spontaneously enter into bacteria. The intracellular sDNA associated themselves with host cell chromosomes and integrated into their genomes. Furthermore, sDNA, but not HMW DNA, from all four sources could phosphorylate H2AX and activate the pro-inflammatory transcription factor NFκB in mouse cells, indicating that sDNAs had acquired biological activities.

Our results show that small fragments of DNA from different sources can indiscriminately enter into other cells across species and kingdom boundaries to integrate into their genomes and activate biological processes. This raises the possibility that fragmented DNA that are generated following organismal cell-death may have evolutionary implications by acting as mobile genetic elements that are involved in horizontal gene transfer.

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物理剪切赋予DNA生物活性和跨越物种和王国边界水平传递自身的能力
我们最近报道了在血液中循环的来自死亡细胞的无细胞DNA (cfDNA)片段是生物活性分子,可以很容易地进入健康细胞,激活受体的DNA损伤和凋亡反应。然而,传统上并不知道DNA会自发地进入细胞或具有任何内在的生物活性。我们假设细胞进入和获得生物学特性是DNA大小的功能。为了验证这一假设,我们通过超声高分子量DNA (HMW DNA)来模拟循环cfDNA来产生小的DNA片段。从癌变和非癌变的人类细胞、细菌和植物中分离的HMW DNA超声产生的片段300-3000 ?bp的大小与报道的循环cfDNA相似。我们在这里表明,虽然HMW DNA不能进入细胞,但来自不同来源的声波DNA (sDNA)可以不受物种或王国边界的影响而不加选择地进入细胞。因此,来自人类细胞、细菌和植物的sDNA可以进入小鼠细胞核,来自人类、细菌和植物的sDNA可以自发进入细菌。细胞内的sDNA与宿主细胞染色体结合并整合到宿主细胞的基因组中。此外,四种来源的sDNA,而不是HMW DNA,都能使小鼠细胞中的H2AX磷酸化并激活促炎转录因子NFκB,这表明snas已获得生物活性。我们的研究结果表明,来自不同来源的DNA小片段可以不分青红皂白地进入跨越物种和王国边界的其他细胞,整合到它们的基因组中并激活生物过程。这就提出了这样一种可能性,即有机体细胞死亡后产生的片段化DNA可能作为参与水平基因转移的移动遗传元素而具有进化意义。
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来源期刊
BMC Molecular Biology
BMC Molecular Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: BMC Molecular Biology is an open access journal publishing original peer-reviewed research articles in all aspects of DNA and RNA in a cellular context, encompassing investigations of chromatin, replication, recombination, mutation, repair, transcription, translation and RNA processing and function.
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