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ela ela
wrote...
11 years ago
What are RFLPs, VNTRs, and SNPs? What is the relationship among these? How do we use this technology to, for example, identify paternity?
                
                
                
                
                
                
                
 
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bio_manbio_man
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11 years ago
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the f,  Caera Dennehy

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wrote...
11 years ago
Hey, Ela. Have you turned this in yet? Was it correct?
wrote...
11 years ago
Did you ever find out the correct answer to this?
wrote...
11 years ago
DNA banding patterns that result from electrophoresis and the subsequent use of a specific cDNA probe during Southern Blotting, can indicate the types of VNTRs and SNPs that are present in the DNA. These DNA fingerprints may be used in a number of ways including forensic analysis, disease detection, paternity cases, and evolutionary studies.
 When an individual’s DNA is cut with restriction enzymes and analyzed, differently sized restriction fragments may be produced due to mutations in restriction sites that prevent cutting. These mutations are called SNPs (Single Nucleotide Polymorphisms) and produce differently sized fragments of DNA called RFLPs (Restriction Fragment Length Polymorphisms). Since individuals contain different SNPs and produce different RFLPs, DNA may be cut with a series of different enzymes and analyzed using electrophoresis and Southern blotting. The different banding patterns that are produced may indicate the presence of specific mutations in a DNA sample. This type of DNA fingerprint analysis is used in examining DNA left at crime scenes as well as in detecting genetic diseases that are due to specific mutations.
 Example:
 If cells are left at a crime scene, PCR is used to amplify the DNA in the cells and the DNA fingerprint of cells left at the scene of the crime may be obtained. If the DNA fingerprint of a suspect matches the DNA fingerprint of the cells left at the crime scene, it may be used as evidence in a trial. Typically, hair follicle cells, blood cells, skin cells, and sperm cells are most commonly left at the scene of a crime.



Interestingly, each individual has two copies of each VNTR region, since there are pairs of homologous chromosomes in cells. One VNTR region is inherited from the mother and one VNTR region is inherited from the father. Due to segregation, independent assortment, and crossover that occur during meiosis, each individual inherits a unique set of VNTR regions. When a child’s DNA fingerprint (banding pattern) is analyzed, all the all bands in his/her banding pattern must correspond either to a band in the DNA fingerprint of the mother or a band in the DNA fingerprint of the father. If a child has a band that is not in the mother’s banding pattern, it must be present in the father’s banding pattern. As a result, DNA fingerprints are of value in solving paternity cases. The only individuals that have identical VNTR regions and the same DNA fingerprints are identical twins, since they arose from the same fertilized egg.
wrote...
11 years ago
Polymorphism:
 A DNA polymorphism is a sequence difference compared to a reference standard that is present in at least 1–2% of a population.
 Polymorphisms can be single bases or thousands of bases.
 Polymorphisms may or may not have phenotypic effects.
 Polymorphisms are found throughout the genome.
 If the location of a polymorphic sequence is known, it can serve as a landmark or marker for locating other genes or genetics regions.
 Each polymorphic marker has different versions or alleles.
 RFLP: restriction fragment length polymorphisms
 VNTR: variable number tandem repeats (8 to >50 base pairs)
 SNP: single-nucleotide polymorphisms
 Restriction fragment sizes are altered by changes in or between enzyme recognition sites.

 restriction fragment length polymorphisms

VNTRs were an important source of RFLP genetic markers used in linkage analysis (mapping) of genomes. Now that many genomes have been sequenced, VNTRs have become essential to forensic crime investigations, via DNA fingerprinting and the CODIS database. When removed from surrounding DNA by the PCR or RFLP methods, and their size determined by gel electrophoresis or Southern blotting, they produce a pattern of bands unique to each individual. When tested with a group of independent VNTR markers, the likelihood of two unrelated individuals having the same allelic pattern is extremely improbable. VNTR analysis is also being used to study genetic diversity and breeding patterns in populations of wild or domesticated animals.

Repetitive DNA, representing over 40% of the human genome, is arranged in a bewildering array of patterns. Repeats were first identified by the extraction of Satellite DNA, which does not reveal how they are organized. The use of restriction enzymes showed that some repeat blocks were interspersed throughout the genome. DNA sequencing later showed that other repeats are clustered at specific locations, with tandem repeats being more common than inverted repeats (which may interfere with DNA replication). VNTRs are the class of clustered tandem repeats that exhibit allelic variation in their lengths

Restriction fragment length polymorphism
 In molecular biology, the term restriction fragment length polymorphism, or RFLP, (commonly pronounced “rif-lip”) refers to a difference between two or more samples of homologous DNA molecules arising from differing locations of restriction sites, and to a related laboratory technique by which these segments can be distinguished. In RFLP analysis the DNA sample is broken into pieces (digested) by restriction enzymes and the resulting restriction fragments are separated according to their lengths by gel electrophoresis. Although now largely obsolete, RFLP analysis was the first DNA profiling technique cheap enough to see widespread application. In addition to genetic fingerprinting, RFLP was an important tool in genome mapping, localization of genes for genetic disorders, determination of risk for disease, and paternity testing.

SNPs that are not in protein-coding regions may still affect gene splicing, transcription factor binding, messenger RNA degradation, or the sequence of non-coding RNA. Gene expression affected by this type of SNP is referred to as an eSNP (expression SNP) and may be upstream or downstream from the gene
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