Why Are There Many Different Types of tRNA Molecules?

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When genes are expressed into proteins, DNA is first transcribed into messenger RNA (mRNA), which is then translated by transfer RNA (tRNA) into a growing chain of amino acids called a polypeptide. Polypeptides are then processed and folded into functional proteins. The complex steps of translation require many different forms of tRNA in order to accommodate the multitudinous variations in the genetic code.

Nucleotides

There are four nucleotides in DNA: adenine, guanine, cytosine and thymine. These nucleotides, also known as bases, are arranged in sets of three called codons. Because there are four amino acids that could comprise each of the three bases in a codon, there are 4^3 = 64 possible codons. Some codons code for the same amino acid, and so the actual number of tRNA molecules needed is less than 64. This redundancy in the genetic code is referred to as "wobble."

Amino Acids

Each codon codes for one amino acid. It is the function of tRNA molecules to translate the genetic code from bases into amino acids. The tRNA molecules accomplish this by binding to a codon on one end of the tRNA and an amino acid on the other end. For this reason, a variety of tRNA molecules are needed in order to accommodate not only the variety of codons but also the different types of amino acids in the body. Humans typically use 20 different amino acids.

Stop Codons

While most codons code for an amino acid, three specific codons trigger the end of polypeptide synthesis rather than coding for the next amino acid in the growing protein. There are three such codons, called stop codons: UAA, UAG and UGA. Thus, in addition to needing tRNA molecules to pair up with each amino acid, an organism needs other tRNA molecules to pair up with the stop codons.

Non-Standard Amino Acids

In addition to the 20 standard amino acids, some organisms use additional amino acids. For example, the selenocysteine tRNA has a somewhat different structure than do other tRNAs. Selenocysteine tRNA initially pairs with serine, which is then converted to selenocysteine. Interestingly, UGA (one of the stop codons) codes for selenocysteine and so assistive molecules are needed to avoid halting protein synthesis when the cell's translation machinery reaches the selenocysteine codon.

References

About the Author

Sly Tutor has been a writer since 2005 and has had work appear in the "Altoona Mirror" newspaper. She holds a Bachelor of Science in microbiology from Pennsylvania State University.

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