1.From the "Out of Africa Theory" Study to the Application of "DNA Biogeographic Ancestry Inference" in Criminal Investigation.
Li JIANG ; Jing LIU ; Cai Xia LI
Journal of Forensic Medicine 2019;35(5):519-524
Genetic markers, such as single nucleotide polymorphism (SNP), insertion/deletion (InDel), were discovered and widely used with the development of whole genome sequencing and bioinformatics technology. The origin and genetic structure of the modern population had been gradually revealed from the perspective of genetics. The study on biogeographic ancestry inference in the field of forensic genetics emerged and developed rapidly, providing clues and scientific basis for the determination of investigation direction and for the narrow of the scope of investigation in the process of case investigation. This paper briefly reviews the research progress, inference methods and development trends of DNA ancestry inference technology.
Africa
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Criminals
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DNA/genetics*
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DNA Fingerprinting/methods*
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Forensic Genetics/methods*
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Genetics, Population
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Humans
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Phylogeography
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Polymorphism, Single Nucleotide
2.Genuineness of Morinda officinalis How germplasm inferred from ITS sequences variation of nuclear ribosomal DNA.
Ping DING ; Jin LIU ; Jin-Ying QIU ; Xiao-Ping LAI
Acta Pharmaceutica Sinica 2012;47(4):535-540
PCR sequencing ITS genes methods were used to assess the genetic diversity of Morinda officinalis How different populations. The sequence of Morinda officinalis ITS gene was 567 bp in length, and the content of G/C was 64.5%. In this study, 17 haplotypes were obtained, which were at a high level of branching, and the haplotypes of Guangdong population showed to be the expansion origin. The result of the analysis of molecular variance (AMOVA) also showed that the percentage of variation among populations (56.65%) was greater than that within a population (43.35%). The F(ST) value was 0.566 5, and the genetic divergence among populations was significant. Mantel test results also indicated that the level of geneflow was positively correlated with geographic distances (R2 = 0.721 1). The result showed a good correlation between genotype and geographic distribution of Morinda officinalis, and ITS gene sequencing could be useful molecular method for the genuineness and phylogeography of Morinda officinalis.
DNA, Ribosomal Spacer
;
genetics
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Gene Flow
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Genetic Variation
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Genetics, Population
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Genotype
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Haplotypes
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Morinda
;
genetics
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Phylogeography
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Polymerase Chain Reaction
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Sequence Analysis, DNA
3.AncestryPainter: A Graphic Program for Displaying Ancestry Composition of Populations and Individuals.
Qidi FENG ; Dongsheng LU ; Shuhua XU
Genomics, Proteomics & Bioinformatics 2018;16(5):382-385
Ancestry composition of populations and individuals has been extensively investigated in recent years due to advances in the genotyping and sequencing technologies. As the number of populations and individuals used for ancestry inference increases remarkably, say more than 100 populations or 1000 individuals, it is usually challenging to present the ancestry composition in a traditional way using a rectangular graph. To address this issue, we developed a program, AncestryPainter, which can illustrate the ancestry composition of populations and individuals with a rounded and nice-looking graph to save space. Individuals are depicted as length-fixed bars partitioned into colored segments representing different ancestries, and the population of interest can be highlighted as a pie chart in the center of the circle plot. In addition, AncestryPainter can also be applied to display personal ancestry in a way similar to that for displaying population ancestry. AncestryPainter is publicly available at http://www.picb.ac.cn/PGG/resource.php.
Computer Graphics
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Genetics, Population
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Humans
;
Software
4.Population genetic study of Magnolia officinalis and Magnolia officinalis var. biloba.
Shengxian YU ; Qingjun YUAN ; Bin YANG ; Chunxia ZHANG ; Chengyu CHEN
China Journal of Chinese Materia Medica 2010;35(16):2129-2132
OBJECTIVEpopulation genetic study of Magnolia officinalis and M. officinalis var. biloba was performed in this paper. The objectives of this study are to provide baseline data of molecular pharmaceutics for quality control of Cortex Magnoliae Officinalis.
METHODA total of 15 populations of M. officinalis and M. officinalis var. biloba were collected. PCR amplification and sequencing were performed with two chloroplast intergenic spacers psbA-trnH and trnL-trnF. Chloroplast haplotype frequencies were calculated, genetic diversity and genetic structure were estimated by using the program HAPLONST, and a haplotype network depicting the mutational relationships among distinct haplotypes was drawn following the principle of parsimony by TCS version 1.13.
RESULTThe differentiation of haplotype frequencies between M. officinalis and M. officiunalis var. biloba was significant although there was no private haplotypes of themselves.
CONCLUSIONThere was certain genetic divergence between M. officinalis and M. offcinalis var. biloba although the monophyletic clade of themselves was not still formed.
Evolution, Molecular ; Genetics, Population ; Haplotypes ; Magnolia ; classification ; genetics
7.Genetic polymorphisms of 15 STR loci in Gansu Hui population.
Hong-Bing SUN ; Xin YANG ; Fei HA ; Ji-Huai LUO ; Zi-Long ZHANG
Journal of Forensic Medicine 2013;29(6):464-471
8.The Biology of Alcohol Dependence.
Journal of the Korean Medical Association 2006;49(2):108-113
Alcohol dependence (AD) is a chronically relapsing disease and has various biological etiologies. Neither genetics nor neurobiology explains the pathogenesis of AD exclusively. AD is a multifactorial disease. This article reviews the genetic and biological aspects of AD. Many candidate genes and neurotransmitters play important roles in AD. Further studies are needed to elucidate the biological mechanisms of AD. Also the treatment of AD should be individualized according to the patients's biological characteristics.
Alcoholism*
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Biology*
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Genetics
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Neurobiology
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Neurotransmitter Agents
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Population Characteristics
9.Genetic and Phenotypic Variation of Campylobacter jejuni NCTC11168 Caused by flhA Mutation during Laboratory Passage.
Xiao Li CHEN ; Hao LIANG ; Peng Bo GUO ; Yi Xin GU ; Jia Qi WANG ; Hai Rui WANG ; Gui Lan ZHOU ; Zhu Jun SHAO ; Jian Zhong ZHANG ; Mao Jun ZHANG
Biomedical and Environmental Sciences 2023;36(7):604-613
OBJECTIVE:
Campylobacter jejuni NCTC11168 is commonly used as a standard strain for flagellar biosynthesis research. In this report, two distinguished phenotypic isolates (CJ1Z, flhA mutant strain, lawn; CJ2S, flhA complemented strain, normal colony) appeared during laboratory passages for NCTC11168.
METHODS:
Phenotypic assessments, including motility plates, transmission electron microscopy, biofilm formation assay, autoagglutination assay, and genome re-sequencing for these two isolates (CJ1Z, flhA mutant strain; CJ2S, flhA complemented strain) were carried out in this study.
RESULTS:
Transmission electron microscopy revealed that the flagellum was lost in CJ1Z. Phenotypic assessments and genome sequencing of the two isolates were performed in this study. The capacity for biofilm formation, colony auto-agglutination, and isolate motility was reduced in the mutant CJ1Z. Comparative genomic analysis indicated a unique native nucleotide insertion in flhA (nt, 2154) that caused the I719Y and I720Y mutations and early truncation in flhA.
CONCLUSION
FlhA has been found to influence the expression of flagella in C. jejuni. To the best of our knowledge, this is the first study to describe the function of the C-terminal of this protein.
Campylobacter jejuni/genetics*
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Bacterial Proteins/metabolism*
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Mutation
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Biological Variation, Population
10.Recent progress of study on single nucleotide polymorphisms.
Dai Xin HUANG ; Lin ZHANG ; Mei Yun WU
Journal of Forensic Medicine 2001;17(2):122-125
Single nucleotide polymorphisms (SNPs) is a new genetic marker system following RFLP and microsatellite polymorphism. It has been shown to have the characteristics of high-density, inheritance stability and facilitation in analysis automation. SNPs can be detected by electrophoresis, endonuclease-cleavage, PCR and sequencing, and can be used extensively in gene mapping, disease-correlativity analysis, population genetics and drug research.
Chromosome Mapping
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Genetic Markers
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Genetics, Population
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Humans
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Polymorphism, Single Nucleotide