In Trypanosoma, some of the introns generate Y shaped structure in place of a lariat. Such structure is generated during
trans-splicing
In molecular biology, gene expression involves several steps, including transcription (creating RNA from DNA) and translation (creating protein from RNA). Before the messenger RNA (mRNA) molecule is ready for translation, it often undergoes modifications, one of which is splicing.
Splicing is the process where non-coding regions, called introns, are removed from the pre-mRNA molecule, and the coding regions, called exons, are joined together. This results in a mature mRNA molecule that can be translated into a functional protein.
There are generally two main types of splicing:
Trypanosoma extensively uses trans-splicing. This process is essential for processing most of its protein-coding genes. In Trypanosomes, many genes are transcribed as polycistronic units (multiple genes on a single RNA molecule). Trans-splicing helps in processing these into individual monocistronic mRNAs, each receiving a common spliced leader sequence at its 5' end.
The mechanism of trans-splicing in Trypanosoma differs from cis-splicing in how the intron is released. During trans-splicing, the intron from the target pre-mRNA molecule and the intron from the SL RNA molecule are released together. The structure formed by these introns is not the typical lariat seen in cis-splicing.
Instead, due to the joining of two separate RNA molecules and the nature of the splicing reaction, the released intron structure resembles a Y shape. This Y-shaped structure is a characteristic intermediate and product of the trans-splicing pathway in organisms like Trypanosoma.
The formation of a Y-shaped intron structure, instead of a lariat, is a distinctive feature of the trans-splicing mechanism widely used in organisms like Trypanosoma for processing their RNA molecules.
Many organisms encode only 18 aminoacyl-tRNA synthetases (aaRS). These organisms lack aaRS that use Asn or Gln (as one of the substrates) for direct aminoacylation of the tRNAAsn and tRNAGln, respectively. Which one of the following statements represents the correct option?
Precise recognition of tRNAs by their cognate aminoacyl‐tRNA synthetases is crucial for the fidelity of protein synthesis. In the context of the aminoacylation of tRNAAla with its cognate aminoacyl‐tRNA synthetase (AlaRS) and based on the studies on the molecules of Escherichia coli origin, following statements are made. Which one of the statements is INCORRECT?
Which one of the following RNAs possesses the peptidyltransferase activity?
Which one of the following statements about GAL gene expression is FALSE?
Which one of the following ensures stable binding of RNA polymerase at the promoter site?