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CRISPR-Cas9 Gene Editing Therapy, a Curative Hope for Sickle Cell in Nigeria, West Africa CRISPR-Cas9 基因编辑疗法,西非尼日利亚镰状细胞病的治愈希望
Pub Date : 2024-07-15 DOI: 10.11648/j.ijgg.20241203.11
Babatunde Olowu, Ahmed Olaide, Oluwaloni Tinubu
Sickle cell anaemia is one of the haemoglobin abnormalities resulting from a genetic mutation— it is caused by inheriting two faulty genes that result in an abnormal substitution of glutamate for valine on the beta chain of haemoglobin, which causes haemoglobin molecules to stick together. According to a World Health Organization (WHO) report, 20 out of every 1,000 births suffer from sickle-cell anaemia, and 24% of Nigerians are carriers of this mutant gene. Scientists have suggested several solutions, including stem cell transplantation and gene therapies, but these have faced opposition due to ethical beliefs, high cost, and the ensuing immune issues. Research is now centered on advancing genome editing techniques for gene therapy. Ongoing studies have proven that genetic differences can be corrected methodically by modifying the genome at specific sites instead of introducing a new copy of the affected gene into the cells; due to the effectiveness of this method, scientists are testing its applications in manipulating genes in various systems. This review correlates a few studies that used the recently developed technique—CRISPR-Cas9—as a novel approach to gene therapy, dissecting the different clinical studies about sickle cell origin to point out many of its ethical and medical limitations, the consequences of these limitations, and the advancements this technology has made possible.
镰状细胞性贫血是基因突变导致的血红蛋白异常之一--它是由于遗传了两个有缺陷的基因,导致血红蛋白β链上的谷氨酸异常取代缬氨酸,从而使血红蛋白分子粘连在一起。根据世界卫生组织(WHO)的一份报告,每 1000 名新生儿中就有 20 人患有镰状细胞贫血症,而 24% 的尼日利亚人是这种突变基因的携带者。科学家们提出了几种解决方案,包括干细胞移植和基因疗法,但由于伦理观念、高昂的费用以及随之而来的免疫问题,这些方案都遭到了反对。目前的研究重点是推进基因组编辑技术,以实现基因治疗。正在进行的研究证明,通过修改基因组的特定位点,而不是在细胞中引入受影响基因的新拷贝,可以有条不紊地纠正基因差异;由于这种方法的有效性,科学家们正在测试其在各种系统中操纵基因的应用。这篇综述关联了几项使用最近开发的技术--CRISPR-Cas9--作为基因治疗新方法的研究,剖析了有关镰状细胞病因的不同临床研究,指出了它在伦理和医学方面的许多局限性、这些局限性的后果以及这项技术所带来的进步。
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引用次数: 0
Evaluation of Coffee Genotype for Drought Tolerance and Water Use Efficiency in Western Ethiopia at West Wollega 在西沃勒加评估埃塞俄比亚西部咖啡基因型的抗旱性和用水效率
Pub Date : 2024-02-21 DOI: 10.11648/j.ijgg.20241201.13
Huluager Ayanaw, Zelalem Tamiru, Minida Tadese, A. Asefa
The growth and output of coffee are significantly hampered by drought. To lessen the effects of climate change on coffee production, it is crucial to choose genotypes of Arabica coffee that are resistant to drought. The goal of the study was to select genotypes of Wellega coffee that are drought-tolerant at the Haru Agricultural Research Sub-Center in the Oromia National Regional State, Western Ethiopia. The experiment was carried out in a controlled environment from 2017 to 2019 G. C., with three replications laid out in RCBD. For 28 days, two watering regimes—well-watered and water-stressed—were applied to fourteen genotypes of Wellega coffee. The mother trees of genotype were tested at field condition. The experiment's findings showed that the genotypes not differed significantly in terms of total dry matter, relative leaf water content, and leaf retention capacity as well as in terms of the degree of wilting and in all destructive parameters. So, to select the drought tolerance coffee genotypes the stress period should be minimized in to 15-21 days.
干旱严重影响了咖啡的生长和产量。为了减轻气候变化对咖啡生产的影响,选择抗旱的阿拉比卡咖啡基因型至关重要。这项研究的目的是在埃塞俄比亚西部奥罗米亚国家区域州的哈鲁农业研究分中心选择耐旱的 Wellega 咖啡基因型。实验于 2017 年至 2019 年在受控环境中进行,采用 RCBD 方式布置了三个重复。在 28 天的时间里,对 14 种 Wellega 咖啡基因型采用了充足浇水和缺水浇水两种浇水制度。基因型的母树在田间进行了测试。实验结果表明,各基因型在总干物质、叶片相对含水量、叶片保持能力以及萎蔫程度和所有破坏性参数方面均无显著差异。因此,要选择耐旱的咖啡基因型,应尽量缩短胁迫期至 15-21 天。
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引用次数: 0
Morphological Variations in Bread Wheat (Triticum aestivum L.) Genotypes in Gechi District, South West Ethiopia 埃塞俄比亚西南部 Gechi 地区面包小麦(Triticum aestivum L.)基因型的形态变异
Pub Date : 2024-01-11 DOI: 10.11648/j.ijgg.20241201.11
Garome Shifaraw, S. Alamerew, Techale Birhan
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引用次数: 0
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International Journal of Genetics and Genomics
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