RNA has 4 different bases: adenine, guanine, cytosine, and uracil. The first 3 bases are the same as those found in DNA, but uracil replaces thymine as the base complementary to adenine. This may be because uracil is energetically less expensive to produce, although it easily degenerates into cytosine. Thus, uracil is appropriate for RNA, where quantity is important but lifespan is not, whereas thymine is appropriate for DNA.
Structurally, RNA is indistinguishable from DNA except for the critical presence (noted above) of an additional hydroxyl group attached to the pentose ring in the 2' position. This additional group gives the molecule far greater catalytic versatility and allows it to perform reactions that DNA is incapable of performing.
The other major difference between RNA and DNA is that RNA is almost exclusively found in the single-stranded form (an exception being the genetic material of some kinds of viruses). RNA molecules often fold into more complex structures by making use of complementary internal sequences; that is, one part of a single RNA molecule is the nucleic acid complement of another part of the same molecule (for exampls, 5'-ACUCGA-3' and 5'-UCGAGU-3', or the palindrome 5'-GCAGACG-3' with 5'-CGUCUGC-3'), so that the two strands bind together. This allows the formation of hairpin loops, coils, etc., which then direct the formation of higher-order structures.
The first life on earth may have been RNA-based, due to RNA's ability both to carry genetic information like DNA and also to catalyze biochemical reactions like enzymes. This possiblity is termed the RNA world hypothesis. Even today, some viruses, such as retroviruses, use RNA as their sole genetic material. RNA is less stable than DNA, however, and is also a less efficient catalyst than a protein-based enzyme. These facts may have led to selection for reduced use of RNA in cells, and greater use of DNA and proteins.
RNA plays several roles in biology:
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mRNA runs through several steps during its usually brief existence: During transcription, an enzyme called RNA polymerase makes a copy of a gene from the DNA to mRNA as needed. In prokaryotes, no further processing of mRNA occurs (except in rare cases), and often translation of the mRNA into protein occurs even while transcription is going on. In eukaryotes, transcription and translation occur in different parts of the cell (transcription in the nucleus, where DNA is kept, and translation in the cytoplasm, where ribosomes reside). Also in eukaryotes, mRNA undergoes several processing steps before it is ready to be translated:
Messenger RNA that has been processed and is ready for transcription is called a "mature transcript" or "mature mRNA" or sometimes simply "mRNA". Unprocessed or partially-processed messenger RNA is called "pre-mRNA" or "hnRNA" (for heteronucleic RNA)
Anti-sense mRNA can inhibit gene translation in many eukaryotes, when the anti-sense RNA's sequence is complementary to that of the mRNA of the gene. This means a gene is not expressed as protein if a matching anti-sense mRNA is present in the cell. This may be a defense mechanism against retroposons (transposons that use dsRNA as an intermediate state) or viruses, because both can use double-stranded mRNA as an intermediate. In biochemical research, this effect has been used to study gene function, simply shutting down the studied gene by adding its anti-sense mRNA transcript. Such studies have been done on the worm C. elegans.
Compare RNA interference.
See RNA gene.
See virus and RNA world hypothesis.
Double-stranded RNA (or dsRNA) is RNA with 2 complementary strands, similar to the DNA found in all "higher" cells. dsRNA forms the genetic material of some viruses (see virus). In eukaryotes, it may play a role in the process of RNA interference and in microRNAs.
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