Examine individual changes

'In [[molecular biology]], the term '''restriction fragment length polymorphism''', or '''RFLP''', (commonly pronounced “rif-lip”) refers to a [[polymorphism (biology)|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 inexpensive enough to see widespread application. In addition to genetic fingerprinting, RFLP was an important tool in [[genome mapping]], localization of genes for [[genetic disorder]]s, determination of [[Genetic testing|risk]] for disease, and [[paternity testing]]. == Analysis technique == The basic technique for detecting RFLPs involves fragmenting a sample of DNA by a [[restriction enzyme]], which can recognize and cut DNA where time [allele]], and can be used in [[Genetics|genetic analysis]]. RFLP analysis may be subdivided into single- (SLP) and multi-locus probe (MLP) paradigms. Usually, the SLP method is preferred over MLP because it is more sensitive, easier to interpret and capable of analyzing mixed-DNA samples.{{Citation needed|date=August 2009}} Moreover data can be generated even when the DNA is degraded (e.g. when it is found in bone remains.) [[File:RFLPDemo1.gif|right|thumb|450px|<center>Schematic for RFLP by cleavage site loss.</center>]] [[File:RFLP genotyping.gif|right|thumb|360px|<center>Analysis and inheritance of allelic RFLP fragments (NIH).</center>]] [[File:RFLPDemo2.gif|right|thumb|450px|<center>Schematic for RFLP by VNTR length variation.</center>]] === Examples === There are two common mechanisms by which the size of a particular restriction fragment can vary. In the first schematic, a small segment of the genome is being detected by a DNA probe (thicker line). In allele "A", the genome is cleaved by a restriction enzyme at three nearby sites (triangles), but only the rightmost fragment will be detected by the probe. In allele "a", restriction site 2 has been lost by a [[genetic mutation|mutation]], so the probe now detects the larger fused fragment running from sites 1 to 3. The second diagram shows how this fragment size variation would look on a Southern blot, and how each allele (two per individual) might be inherited in members of a family. In the third schematic, the probe and restriction enzyme are chosen to detect a region of the genome that includes a variable [[Variable number tandem repeats|VNTR]] segment (boxes). In allele "c" there are five repeats in the VNTR, and the probe detects a longer fragment between the two restriction sites. In allele "d" there are only two repeats in the VNTR, so the probe detects a shorter fragment between the same two restriction sites. Other genetic processes, such as [[Genetic insertion|insertions]], [[Genetic deletion|deletions]], [[Chromosomal translocation|translocations]], and [[Chromosomal inversion|inversions]], can also lead to RFLPs. == Applications == Analysis of RFLP variation in genomes was a vital tool in genome mapping and genetic disease analysis. If researchers were trying to initially determine the chromosomal ___location of a particular disease gene, they would analyze the DNA of members of a family afflicted by the disease, and look for RFLP alleles that show a similar pattern of inheritance as that of the disease (see [[Genetic linkage]]). Once a disease gene was localized, RFLP analysis of other families could reveal who was at risk for the disease, or who was likely to be [[Genetic carrier|carriers]] of the mutant genes. RFLP analysis was also the basis for early methods of [[Genetic fingerprinting]], useful in the identification of samples retrieved from [[forensic|crime]] scenes, in the determination of [[Parental testing|paternity]], and in the characterization of [[genetic diversity]] or breeding patterns in animal populations. == Alternatives == The technique for RFLP analysis is, however, slow and cumbersome. It requires a large amount of sample DNA, and the combined process of probe labeling, DNA fragmentation, electrophoresis, blotting, hybridization, washing, and [[autoradiography]] could take up to a month to complete. A limited version of the RFLP method that used [[Oligomer restriction|oligonucleotide probes]] was reported in 1985<ref name="Saiki1">{{cite journal| url=http://sunsite.berkeley.edu/cgi-bin/ebind2html/pcr/034| title= Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia| last=Saiki| first= RK| coauthors= Scharf S, Faloona F, Mullis KB, Erlich HA, Arnheim N| journal=[[Science (journal)|Science]]| year= 1985| month= Dec 20| volume=230| issue=4732| pages=1350–4| doi= 10.1126/science.2999980| pmid= 2999980}}</ref>. Fortunately, the results of the [[Human Genome Project]] have largely replaced the need for RFLP mapping, and the identification of many [[single-nucleotide polymorphism]]s (SNPs) in that project (as well as the direct identification of many disease genes and mutations) has replaced the need for RFLP disease linkage analysis (see [[SNP genotyping]]). The analysis of VNTR alleles continues, but is now usually performed by [[polymerase chain reaction]] (PCR) methods. For example, the standard [[National DNA database|protocols]] for [[DNA fingerprinting]] involve PCR analysis of [[CODIS|panels]] of more than a dozen VNTRs. RFLP is still a technique used in marker assisted selection. Terminal restriction fragment length polymorphism (TRFLP or sometimes T-RFLP) is a [[molecular biology]] technique initially developed for characterizing bacterial communities in mixed-species samples. The technique has also been applied to other groups including soil fungi. TRFLP works by PCR amplification of DNA using primer pairs that have been labeled with fluorescent tags. The PCR products are then digested using RFLP enzymes and the resulting patterns visualized using a DNA sequencer. The results are analyzed either by simply counting and comparing bands or peaks in the TRFLP profile, or by matching bands from one or more TRFLP runs to a database of known species. The technique is similar in some aspects to [[DGGE]] or TGGE. The sequence changes directly involved with an RFLP can also be analyzed more quickly by PCR. Amplification can be directed across the altered restriction site, and the products digested with the restriction enzyme. This method has been called [[Cleaved Amplified Polymorphic Sequence]] (CAPS). Alternatively, the amplified segment can by analyzed by [[Allele specific oligonucleotide]] (ASO) probes, a process that can often be done by a simple [[Dot blot]]. ==See also== *[[STR analysis]] *[[AFLP]] ==External links== your moms anus.com == References == <references/> {{DEFAULTSORT:Restriction Fragment Length Polymorphism}} [[Category:Genomics]] [[ar:تعدد أطوال جزء الحصر]] [[ca:Polimorfisme de longitud del fragment de restricció]] [[cs:Polymorfismus délky restrikčních fragmentů]] [[de:Restriktionsfragmentlängenpolymorphismus]] [[es:Polimorfismos de longitud de fragmentos de restricción]] [[fr:Polymorphisme de longueur des fragments de restriction]] [[id:Polimorfisme Panjang Berkas Restriksi]] [[it:RFLP]] [[ja:RFLP]] [[no:RFLP]] [[pl:Analiza długości fragmentów restrykcyjnych]] [[ru:Полиморфизм длин рестрикционных фрагментов]] [[uk:Поліморфізм довжини рестрикційних фрагментів]] [[vi:Kỹ thuật RFLP]] [[zh:限制性片段長度多態性]]'