Until about 20 years ago, all known enzymes were proteins. But then it was discovered that some RNA molecules can act as enzymes; that is, catalyze covalent changes in the structure of substrates (most of which are also RNA molecules). Catalytic RNA molecules are called ribozymes.Most classes of RNA
All living things — bacteria, archaea, and eukaryotes — synthesize an enzyme called Ribonuclease P (RNase P). It cleaves the head (5') end of the precursors of transfer RNA (tRNA) molecules.In bacteria, ribonuclease P is a heterodimer containing
The splicing reaction is self-contained; that is, the intron — with the help of associated proteins — splices itself out of the precursor RNA.
Once excision of the intron and splicing of the adjacent exons are completed, the story is over. In other words, although the action is catalyzed by the RNA, only a single molecule of substrate is involved (unlike protein enzymes that repeatedly catalyze a reaction).However, synthetic versions of Group I introns made in the laboratory can — in vitro — act repeatedly; that is, like true enzymes.
The DNA of some Group I introns includes an open reading frame (ORF) that encodes a transposase-like protein that can make a copy of the intron and insert it elsewhere in the genome.
|Link to a discussion of transposons.|
All the Group I introns share a characteristic secondary structure and mode of action that distinguishes them from the next group.
Because their secondary structure and the details of the splicing reaction differ from the rRNA introns discussed above, these are called Group II introns.
The DNA of some Group II introns also includes an open reading frame (ORF) that encodes a transposase-like protein that can make a copy of the intron and insert it elsewhere in the genome.
Spliceosomes remove introns and splice the exons of most nuclear genes. They are composed of 5 kinds of small nuclear RNA (snRNA) molecules and over 100 different protein molecules. It is the RNA — not the protein — that catalyzes the splicing reactions.
The molecular details of the reactions are similar to those of Group II introns, and this has led to speculation that this splicing machinery evolved from them.
Both viroids and virusoids are responsible for a number of serious diseases of economically important plants; e.g. the coconut palm and chrysanthemums. (The problem is so severe with chrysanthemums that all growers in the U.S. now secure their stock from a few companies that raise the plants in "clean" rooms using stringent precautions to prevent infection by the viroid.)
But if RNA can serve both as a
Is there evidence that RNA alone can catalyze the synthesis of proteins?
Yes, the ribosome turns out to be a ribozyme.
Ribosomes are huge aggregates containing 3 (4 in eukaryotes) rRNA molecules and scores of protein molecules.
The three-dimensional structure of the large (50S) subunit of a bacterial ribosome was published in August 2000. It clearly shows that formation of the peptide bond that links each amino acid to the growing polypeptide chain is catalyzed by the 23S RNA molecule in the large subunit. The 31 proteins in the subunit probably provide the scaffolding needed to maintain the three-dimensional structure of the RNA.
|Link to discussion of ribosome structure and function.|
In today's world, RNA polymerases — made of protein — make the RNA molecules (using the antisense strand of DNA as a template [View]). Could RNA alone have done it?
It can be done in the laboratory. Wochner, A. et al. reported in Science, 332:209, 8 April 2011, their creation of a synthetic RNA molecule that when presented with single-stranded RNA templates, polymerizes ribonucleotide triphosphates into strands of RNA complementary to the template. Their synthetic RNA polymerase was able to faithfully incorporate up to 95 nucleotides into complementary strands of RNA. One product was a functional endonuclease ribozyme. (By the autumn of 2013, they were able to copy a template of 206 nucleotides.)
The ability of ribozymes to recognize and cut specific RNA molecules makes them exciting candidates for human therapy. Already, a synthetic ribozyme that destroys the mRNA encoding a receptor of Vascular Endothelial Growth Factor (VEGF) is being readied for clinical trials. VEGF is a major stimulant of angiogenesis, and blocking its action may help starve cancers of their blood supply.
|Link to discussion of angiogenesis inhibitors and cancer.|