Nucleic acid hybridization

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In molecular biology, hybridization (or hybridisation) is a phenomenon in which single-stranded deoxyribonucleic acid (DNA) or ribonucleic acid (RNA) molecules anneal to complementary DNA or RNA.[1] Though a double-stranded DNA sequence is generally stable under physiological conditions, changing these conditions in the laboratory (generally by raising the surrounding temperature) will cause the molecules to separate into single strands. These strands are complementary to each other but may also be complementary to other sequences present in their surroundings. Lowering the surrounding temperature allows the single-stranded molecules to anneal or “hybridize” to each other.

DNA replication and transcription of DNA into RNA both rely upon nucleotide hybridization, as do molecular biology techniques including Southern blots and Northern blots,[2] the polymerase chain reaction (PCR), and most approaches to DNA sequencing.

Applications[edit]

Hybridization is a basic property of nucleotide sequences and is taken advantage of in numerous molecular biology techniques. Overall genetic relatedness of two species can be determined by hybridizing segments of their DNA (DNA-DNA hybridization). Due to sequence similarity between closely related organisms, higher temperatures are required to melt such DNA hybrids when compared to more distantly related organisms. A variety of different methods use hybridization to pinpoint the origin of a DNA sample, including the polymerase chain reaction (PCR). In another technique, short DNA sequences are hybridized to cellular mRNAs to identify expressed genes. Pharmaceutical drug companies are exploring the use of antisense RNA to bind to undesired mRNA, preventing the ribosome from translating the mRNA into protein.[3]

DNA-DNA hybridization[edit]

For more details on this topic, see DNA-DNA hybridization.

Fluorescence In Situ Hybridization[edit]

For more details on this topic, see Fluorescence in situ hybridization.

Fluorescence in situ hybridization (FISH) is a laboratory method used to detect and locate a DNA sequence, often on a particular chromosome.[4]

Researchers Joseph Gall and Mary Lou Pardue realized in the 1960's that molecular hybridization could be used to identify the position of DNA sequences in situ (i.e., in their natural positions within a chromosome). In 1969, the two scientists published a paper demonstrating that radioactive copies of a ribosomal DNA sequence could be used to detect complementary DNA sequences in the nucleus of a frog egg.[5] Since those original observations, many refinements have increased the versatility and sensitivity of the procedure to the extent that in situ hybridization is now considered an essential tool in cytogenetics.

References[edit]

  1. ^ Felsenfeld, G; Miles, HT (1967). "The physical and chemical properties of nucleic acids.". Annual review of biochemistry 36: 407–48. PMID 18257727. 
  2. ^ http://www.ndsu.edu/pubweb/~mcclean/plsc731/dna/dna6.htm Southern and Northern blotting
  3. ^ http://www.biologyreference.com/Ho-La/Hybridization.html
  4. ^ Levsky, JM; Singer, RH (15 July 2003). "Fluorescence in situ hybridization: past, present and future.". Journal of cell science 116 (Pt 14): 2833–8. doi:10.1242/jcs.00633. PMID 12808017. 
  5. ^ Pardue, ML; Gall, JG (October 1969). "Molecular hybridization of radioactive DNA to the DNA of cytological preparations.". Proceedings of the National Academy of Sciences of the United States of America 64 (2): 600–4. PMID 5261036. 

External links[edit]