塞内加尔妇女子宫肌瘤Med12外显子2基因结构和突变不稳定性的预测

Kénémé Bineta, Cissé Daouda, Ka Sidy, D. Ahmadou, S. Mbacke, S. Gueye
{"title":"塞内加尔妇女子宫肌瘤Med12外显子2基因结构和突变不稳定性的预测","authors":"Kénémé Bineta, Cissé Daouda, Ka Sidy, D. Ahmadou, S. Mbacke, S. Gueye","doi":"10.11648/J.IJGG.20190703.18","DOIUrl":null,"url":null,"abstract":"Uterine fibroids are benign proliferations of slow evolution. They are associated with significant morbidity and constitute a real public health problem. Despite the large-scale medical and financial burden posed by uterine fibroids, the functional roles of the various factors and genes involved in their etiology and growth remain unclear. This shows a great need to undertake a study that would evaluate the molecular features of uterine fibroids. It is in this context that our study is based on 50 Senegalese women with uterine fibroids. Samples of tumour tissue and blood were taken from each patient. After sequencing, the raw data was submitted to the Mutation Surveyor software version 5.0.1. Pathogenicity of mutations was evaluated with Polyphen software. To better understand the functional impact of missense mutations at the three-dimensional level, we simulated the structure of the protein by the ab-initio method using the I-Tasser web server. After cleaning, correcting and aligning the sequences with the BioEdit software version 8.0.5, the amino acid frequencies for the blood and tumour tissue samples were retrieved with the MEGA7 software. To see if there is a difference in the distribution of each amino acid between blood and tumour tissue, the average comparison test was performed with the R software version 3.3.1. Our results showed the presence of mutations of the MED12 gene only in tumour tissues. All mutations are predicted to be deleterious. In comparison to the reference sequence, all the mutations show a conformational change in the 3D structure of the MED12 protein. In addition, the mutations p. Q43P, p. G44S, p. G44D, p. G44R, p. F45V, p. K60M give proteins of α-β structure different from the reference sequence which has an α structure. All mutations alter the predicted function of the MED12 protein, which further suggests their involvement in the pathobiology of uterine fibroids in Senegalese women. With regard to amino acid frequencies, the comparison of means between blood and tumour tissue samples shows different distributions for amino acids such as cysteine, aspartic acid, glycine, histidine, leucine, arginine and serine. The results obtained make it possible to better understand the molecular mechanisms involved in the etiology of uterine fibroids. They allow glimpsing applications for the screening of populations at risk, for a non-invasive diagnosis or even for preventive or curative treatment.","PeriodicalId":88902,"journal":{"name":"International journal of genetics and molecular biology","volume":"46 1","pages":"80"},"PeriodicalIF":0.0000,"publicationDate":"2019-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Prediction of the Structure and Mutations Instability of the Med12 Exon2 Gene in Uterine Fibroids in Senegalese Women\",\"authors\":\"Kénémé Bineta, Cissé Daouda, Ka Sidy, D. Ahmadou, S. Mbacke, S. Gueye\",\"doi\":\"10.11648/J.IJGG.20190703.18\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Uterine fibroids are benign proliferations of slow evolution. They are associated with significant morbidity and constitute a real public health problem. Despite the large-scale medical and financial burden posed by uterine fibroids, the functional roles of the various factors and genes involved in their etiology and growth remain unclear. This shows a great need to undertake a study that would evaluate the molecular features of uterine fibroids. It is in this context that our study is based on 50 Senegalese women with uterine fibroids. Samples of tumour tissue and blood were taken from each patient. After sequencing, the raw data was submitted to the Mutation Surveyor software version 5.0.1. Pathogenicity of mutations was evaluated with Polyphen software. To better understand the functional impact of missense mutations at the three-dimensional level, we simulated the structure of the protein by the ab-initio method using the I-Tasser web server. After cleaning, correcting and aligning the sequences with the BioEdit software version 8.0.5, the amino acid frequencies for the blood and tumour tissue samples were retrieved with the MEGA7 software. To see if there is a difference in the distribution of each amino acid between blood and tumour tissue, the average comparison test was performed with the R software version 3.3.1. Our results showed the presence of mutations of the MED12 gene only in tumour tissues. All mutations are predicted to be deleterious. In comparison to the reference sequence, all the mutations show a conformational change in the 3D structure of the MED12 protein. In addition, the mutations p. Q43P, p. G44S, p. G44D, p. G44R, p. F45V, p. K60M give proteins of α-β structure different from the reference sequence which has an α structure. All mutations alter the predicted function of the MED12 protein, which further suggests their involvement in the pathobiology of uterine fibroids in Senegalese women. With regard to amino acid frequencies, the comparison of means between blood and tumour tissue samples shows different distributions for amino acids such as cysteine, aspartic acid, glycine, histidine, leucine, arginine and serine. The results obtained make it possible to better understand the molecular mechanisms involved in the etiology of uterine fibroids. They allow glimpsing applications for the screening of populations at risk, for a non-invasive diagnosis or even for preventive or curative treatment.\",\"PeriodicalId\":88902,\"journal\":{\"name\":\"International journal of genetics and molecular biology\",\"volume\":\"46 1\",\"pages\":\"80\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International journal of genetics and molecular biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.11648/J.IJGG.20190703.18\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of genetics and molecular biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.11648/J.IJGG.20190703.18","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

子宫肌瘤是一种缓慢进化的良性增生。它们与严重的发病率有关,构成了一个真正的公共卫生问题。尽管子宫肌瘤造成了大规模的医疗和经济负担,但涉及其病因和生长的各种因素和基因的功能作用仍不清楚。这表明进行子宫肌瘤分子特征研究的必要性。正是在这种背景下,我们的研究是基于50塞内加尔妇女子宫肌瘤。从每位患者身上抽取肿瘤组织和血液样本。测序后,原始数据提交给变异测量者软件版本5.0.1。用Polyphen软件评价突变的致病性。为了更好地了解错义突变在三维水平上的功能影响,我们利用I-Tasser web服务器通过ab-initio方法模拟了该蛋白的结构。使用BioEdit软件8.0.5版本对序列进行清洗、校正和比对后,使用MEGA7软件检索血液和肿瘤组织样本的氨基酸频率。为了观察血液和肿瘤组织中各氨基酸的分布是否存在差异,采用3.3.1版本的R软件进行平均对比检验。我们的研究结果显示MED12基因的突变只存在于肿瘤组织中。所有的突变都被认为是有害的。与参考序列相比,所有突变都显示出MED12蛋白三维结构的构象变化。此外,p. Q43P、p. G44S、p. G44D、p. G44R、p. F45V、p. K60M突变产生的α-β结构蛋白与α结构的参考序列不同。所有突变都改变了MED12蛋白的预测功能,这进一步表明它们参与了塞内加尔妇女子宫肌瘤的病理生物学。在氨基酸频率方面,血液和肿瘤组织样本的平均值比较显示,半胱氨酸、天冬氨酸、甘氨酸、组氨酸、亮氨酸、精氨酸和丝氨酸等氨基酸的分布不同。这些结果使我们能够更好地了解子宫肌瘤发病的分子机制。它们可以用于筛查高危人群,进行非侵入性诊断,甚至进行预防性或治疗性治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Prediction of the Structure and Mutations Instability of the Med12 Exon2 Gene in Uterine Fibroids in Senegalese Women
Uterine fibroids are benign proliferations of slow evolution. They are associated with significant morbidity and constitute a real public health problem. Despite the large-scale medical and financial burden posed by uterine fibroids, the functional roles of the various factors and genes involved in their etiology and growth remain unclear. This shows a great need to undertake a study that would evaluate the molecular features of uterine fibroids. It is in this context that our study is based on 50 Senegalese women with uterine fibroids. Samples of tumour tissue and blood were taken from each patient. After sequencing, the raw data was submitted to the Mutation Surveyor software version 5.0.1. Pathogenicity of mutations was evaluated with Polyphen software. To better understand the functional impact of missense mutations at the three-dimensional level, we simulated the structure of the protein by the ab-initio method using the I-Tasser web server. After cleaning, correcting and aligning the sequences with the BioEdit software version 8.0.5, the amino acid frequencies for the blood and tumour tissue samples were retrieved with the MEGA7 software. To see if there is a difference in the distribution of each amino acid between blood and tumour tissue, the average comparison test was performed with the R software version 3.3.1. Our results showed the presence of mutations of the MED12 gene only in tumour tissues. All mutations are predicted to be deleterious. In comparison to the reference sequence, all the mutations show a conformational change in the 3D structure of the MED12 protein. In addition, the mutations p. Q43P, p. G44S, p. G44D, p. G44R, p. F45V, p. K60M give proteins of α-β structure different from the reference sequence which has an α structure. All mutations alter the predicted function of the MED12 protein, which further suggests their involvement in the pathobiology of uterine fibroids in Senegalese women. With regard to amino acid frequencies, the comparison of means between blood and tumour tissue samples shows different distributions for amino acids such as cysteine, aspartic acid, glycine, histidine, leucine, arginine and serine. The results obtained make it possible to better understand the molecular mechanisms involved in the etiology of uterine fibroids. They allow glimpsing applications for the screening of populations at risk, for a non-invasive diagnosis or even for preventive or curative treatment.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Genetic variability, heritability and genetic advance among yield and yield related traits of advanced Tef [Eragrostis tef (Zucc.) Trotter] breeding lines Sequencing of S5 gene in autotetraploid rice japonica and indica to overcome F1 hybrids embryo sac sterility In silico analysis of mutations associated with genetic variability of the strain African cassava mosaic virus (ACMV) in three departments of Cte dIvoire Contribution of cytogenetic and molecular biology in disorders of sex development diagnosis: About 55 cases The Impact of Sequencing Human Genome on Genomic Food & Medicine
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1