Molecular marker

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A molecular marker is a molecule contained within a sample taken from an organism (biological markers) or other matter. It can be used to reveal certain characteristics about the respective source. DNA, for example, is a molecular marker containing information about genetic disorders, genealogy and the evolutionary history of life. Specific regions of the DNA (genetic markers) are used to diagnose the autosomal recessive genetic disorder cystic fibrosis,[1] taxonomic affinity (phylogenetics) and identity (DNA Barcoding). Further, life forms are known to shed unique chemicals, including DNA, into the environment as evidence of their presence in a particular location.[2] Other biological markers, like proteins, are used in diagnostic tests for complex neurodegenerative disorders, such as Alzheimer's disease.[3] Non-biological molecular markers are also used, for example, in environmental studies.[4]

Genetic markers[edit]

In genetics, a molecular marker (identified as genetic marker) is a fragment of DNA that is associated with a certain location within the genome. Molecular markers are used in molecular biology and biotechnology to identify a particular sequence of DNA in a pool of unknown DNA.

Types of genetic markers[edit]

There are many types of genetic markers, each with particular limitations and strengths. Within genetic markers there are three different categories: "First Generation Markers", "Second Generation Markers", and "New Generation Markers".[5] These types of markers may also identify dominance and co-dominance within the genome.[6] Identifying dominance and co-dominance with a marker may help identify heterozygotes from homozygotes within the organism. Co-dominant markers are more beneficial because they identify more than one allele thus enabling someone to follow a particular trait through mapping techniques. These markers allow for the amplification of particular sequence within the genome for comparison and analysis.

Molecular markers are effective because they identify an abundance of genetic linkage between identifiable locations within a chromosome and are able to be repeated for verification. They can identify small changes within the mapping population enabling distinction between a mapping species, allowing for segregation of traits and identity. They identify particular locations on a chromosome, allowing for physical maps to be created. Lastly they can identify how many alleles an organism has for a particular trait (bi allelic or poly allelic).[7]

List of Markers Acronym
Restriction Fragment Length Polymorphism RFLP
Random Amplified Polymorphic DNA RAPD
Amplified Fragment Length Polymorphism AFLP
VVariable Number Tandem Repeat) VNTR
Oligonucleotide Polymorphism OP
Random Amplified Polymorphic DNA RAPD
Single Nucleotide Polymorphism SNP
Allele Specific Associated Primers ASAP
Inverse Sequence-tagged Repeats ISTR
Inter-retrotransposon Amplified Polymorphism IRAP

Genomic markers as mentioned, have particular strengths and weakness, so, consideration and knowledge of the markers is necessary before use. For instance, a RAPD marker is dominant (identifying only one band of distinction) and it may be sensitive to reproducible results. This is typically due to the conditions in which it was produced. RAPD's are used also under the assumption that two samples share a same locus when a sample is produced.[6] Different markers may also require different amounts of DNA. RAPD's may only need 0.02g of DNA while an RFLP marker may require 10g of DNA extracted from it to produce identifiable results.[8]

Mapping of genetic markers[edit]

Molecular mapping aids in identifying the location of particular markers within the genome. There are two types of maps that may be created for analysis of genetic material. First, is a physical map, that helps identify the location of where you are on a chromosome as well as which chromosome you are on. Secondly there is a linkage map that identifies how particular genes are linked to other genes on a chromosome. This linkage map may identify distances from other genes using (cM) centiMorgans as a unit of measurement. Co-dominant markers can be used in mapping, to identify particular locations within a genome and can represent differences in phenotype.[9] Linkage of markers can help identify particular polymorphisms within the genome. These polymorphisms indicate slight changes within the genome that may present nucleotide substitutions or rearrangement of sequence.[10] When developing a map it is beneficial to identify several polymorphic distinctions between two species as well as identify similar sequence between two species.

Application in plant sciences[edit]

When using molecular markers to study the genetics of a particular crop, it must be remembered that markers have restrictions. It should first be assessed what the genetic variability is within the organism being studied. Analyze how identifiable particular genomic sequence, near or in candidate genes. Maps can be created to determine distances between genes and differentiation between species.[11]

Genetic markers can aid in the development of new novel traits that can be put into mass production. These novel traits can be identified using molecular markers and maps. Particular traits such as color, may be controlled by just a few genes. Qualitative traits (requires less that 2 genes) such as color, can be identified using MAS (marker assisted selection). Once a desired marker is found, it is able to be followed within different filial generations. An identifiable marker may help follow particular traits of interest when crossing between different genus or species, with the hopes of transferring particular traits to offspring.

One example of using molecular markers in identifying a particular trait within a plant is, Fusarium head blight in wheat. Fusarium head blight can be a devastating disease in cereal crops but certain varieties or offspring or varieties may be resistant to the disease. This resistance is inferred by a particular gene that can be followed using MAS (Marker Assisted Selection) and QTL (Quantitative Trait Loci).[12] QTL's identify particular variants within phenotypes or traits and typically identify where the GOI (Gene of interest) is located. Once the cross has been made, sampling of offspring may be taken and evaluated to determine which offspring inherited the traits and which offspring did not. This type of selection is becoming more beneficial to breeders and farmers because it is reducing the amount of pesticides, fungicides and insecticides.[12] Another way to insert a GOI is through mechanical or bacterial transmission. This is more difficult but may save time and money.

Applications of markers in cereal breeding[edit]

  1. Assessing variability of genetic differences and characteristics within a species
  2. Identification and fingerprinting of genotypes
  3. Estimating distances between species and offspring
  4. Identifying location of QTL's
  5. Identification of DNA sequence from useful candidate genes[12]

Application[edit]

It has 5 applications in fisheries and aquaculture:

  1. Species Identification
  2. Genetic variation and population structure study in natural populations
  3. Comparison between wild and hatchery populations
  4. Assessment of demographic bottleneck in natural population
  5. Propagation assisted rehabilitation programmes.However,there still exists some limitations.[13]

Biochemical Markers[edit]

Non-Biological Markers[edit]

See also[edit]

References[edit]

  1. ^ Bradley, Linda A.; Johnson, Dorene A.; Chaparro, Carlos A.; Robertson, Nancy H.; Ferrie, Richard M. (January 1998). "A Multiplex ARMS Test for 10 Cystic Fibrosis (CF) Mutations: Evaluation in a Prenatal CF Screening Program". Genetic Testing 2 (4): 337–341. doi:10.1089/gte.1998.2.337. 
  2. ^ Zimmer, Carl (January 22, 2015). "Even Elusive Animals Leave DNA, and Clues, Behind". New York Times. Retrieved January 23, 2015. 
  3. ^ Choe, Leila H.; Dutt, Michael J.; Relkin, Norman; Lee, Kelvin H. (July 23, 2002). "Studies of potential cerebrospinal fluid molecular markers for Alzheimer's disease". Electrophoresis 23 (14): 2247–2251. doi:10.1002/1522-2683(200207)23:14<2247::aid-elps2247>3.0.co;2-m. PMID 12210229. 
  4. ^ Fraser, M.P.; Yue, Z.W.; Buzcu, B. (May 2003). "Source apportionment of fine particulate matter in Houston, TX, using organic molecular markers". Atmospheric Environment 37 (15): 2117–2123. doi:10.1016/S1352-2310(03)00075-X. 
  5. ^ Maheswaran, M. (2004). "Molecular Markers: History, Features and Applications". Department of Plant Molecular Biology and Biotechnology. 
  6. ^ a b "Traditional Molecular Markers - eXtension". articles.extension.org. Retrieved 2015-12-13. 
  7. ^ Maheswaran, M. (August 2014). "Molecular Markers: History, Features and Applications". Advanced Biotech. 
  8. ^ "Molecular Breeding and Marker-Assisted Selection". International Service For The Acquisition of Agri-Biotech Applications. ISAAA. Retrieved 2015-12-12. 
  9. ^ Griffiths, Anthony JF; Miller, Jeffrey H.; Suzuki, David T.; Lewontin, Richard C.; Gelbart, William M. (2000-01-01). "Mapping with molecular markers". 
  10. ^ "Molecular Linkage Maps". forages.oregonstate.edu. Retrieved 2015-12-13. 
  11. ^ "Molecular breeding and marker-assisted selection". International Service For The Acquisition of Agri-Biotech Applications. ISAAA. Retrieved 2015-12-12. 
  12. ^ a b c Korzun, Viktor. "Molecular markers and their applications in cereals breeding" (PDF). Session I: MAS in Plants. Retrieved 2015-12-12. 
  13. ^ "Molecular markers and their applications in fisheries and aquaculture". Advances in Bioscience and Biotechnology (Scientific Research) 1 (4): 281–291. doi:10.4236/abb.2010.14037. ISSN 2156-8456. Retrieved 5 Dec 2012.