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Encyclopedia > CDNA

In genetics, complementary DNA (cDNA) is single-stranded DNA synthesized from a mature mRNA template. cDNA is often used to clone eukaryotic genes in prokaryotes.

Contents

Overview

The central dogma of genetics outlines that in synthesizing proteins, DNA is transcribed into mRNA, which is translated into protein. One difference between eukaryotic and prokaryotic mRNA is that eukaryotic mRNA can contain introns (intervening sequences), which are not coding sequences, per se, and must be spliced out of the mRNA before it is translated into protein. Prokaryotic mRNA has no introns, so it is not subject to splicing.


Often it is desirable to express eukaryotic genes in prokaryotic cells. A simplified method of doing so would include the addition of eukaryotic DNA to a prokaryotic host, which would transcribe the DNA to mRNA and then translate it to protein. However, as eukaryotic DNA has introns, and since prokaryotes lack the machinery to splice them, the splicing of eukaryotic DNA must be done prior to adding the eukaryotic DNA into the host (as well, before placing the eukaryotic DNA into the prokaryote, it must be methylated and a prokaryotic promoter region must be added). This spliced DNA is called complementary DNA.


Synthesis

Though there are several methods for doing so, cDNA is most often synthesized from mature (fully spliced) mRNA using the enzyme reverse transcriptase. This enzyme operates on a single strand of mRNA, generating its complementary DNA based on the pairing of RNA base pairs (A, U, G, C) to their DNA complements (T, A, C, G).


To obtain eukaryotic DNA whose introns have been spliced:

  1. A eukaryotic cell transcribes the DNA into mRNA.
  2. The same cell processes the nascent mRNA strand by splicing out introns, and adding a poly_A tail and GTP cap.
  3. This mature mRNA strand is extracted from the cell.
  4. A poly_T oligonucleotide is hybridized onto the poly_A tail of the mature mRNA. (Reverse transcriptase requires a double_stranded sequence of nucleic acid to operate; this is often provided by hybridizing a short poly_T oligonucleotide to the poly-A tail of the mature mRNA template. The double-stranded segment serves as a primer for reverse transcriptase.)
  5. Reverse transcriptase is added, along with deoxynucleotide triphosphates (A, T, G, C).

The reverse transcriptase scans the mature mRNA and synthesizes a sequence of DNA that complements the mRNA template. This strand of DNA is complementary DNA.


Applications

Complementary DNA is often used in gene cloning or as gene probes or in the creation of a cDNA library.


External links

  • H-Invitational Database (http://www.h-invitational.jp/)





  Results from FactBites:
 
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cDNAs representing the a-, a'- and d-type mRNAs of HPV-16 (Fig.
The polycistronic cDNAs (d, a and a') were transfected at molar amounts equivalent to 2 (lanes 1) and 0·5 µg (lanes 2) of the monocistronic pJS55-E2 plasmid (E2) together with 2 µg (Cf2Th) or 6 µg (C33A) of the LCR–CAT plasmid and 1 µg of the ß-gal plasmid.
Determination of the transcription-modulatory activities of the monocistronic cDNAs E6I, E7 and E1C towards the HPV-16 LCR (a) and effect of the E1C cDNA on the E2-mediated transcription-modulatory activity (b) in Cf2Th cells.
About Construction of Full-Length cDNAs (397 words)
Construction of full-length cDNAs is a central focus in the post-sequence era of the various genome projects, including Arabidopsis.
However, it is generally agreed upon that a cDNA comprising the entire coding sequence of a protein should be considered worthy for full-length sequencing at high accuracy.
All three investigators have constructed numerous cDNA libraries during the last 20 years in a variety of vectors that are available to the Arabidopsis community.
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