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Give the code and 2 names for each, except the middle one, just one named for …

In bacteria, multiple tRNAs are often transcribed as a single RNA.

Spliceosomes recognize sequences at the 5′ end of the intron because introns always start with the nucleotides GU and they recognize sequences at the 3′ end of the intron because they always end with the nucleotides AG.

In bacteria, multiple tRNAs are often transcribed as a single RNA. The 60S subunit is composed of the 28S rRNA, 5.8S rRNA, 5S rRNA, and 50 proteins. In eukaryotes, pre-rRNAs are transcribed, processed, and assembled into ribosomes in the nucleolus, while pre-tRNAs are transcribed and processed in the nucleus and then released into the cytoplasm where they are linked to free amino acids for protein synthesis.Outline the steps of pre-mRNA processingThe four rRNAs in eukaryotes are first transcribed as two long precursor molecules. DNA replication and RNA transcription and translation. The bacterial large subunit is called the 50S subunit and is composed of the 23S rRNA, 5S rRNA, and 31 proteins, while the bacterial small subunit is called the 30S subunit and is composed of the 16S rRNA and 21 proteins.Eukaryotic pre-mRNA receives a 5′ cap and a 3′ poly (A) tail before introns are removed and the mRNA is considered ready for translation.The tRNAs and rRNAs are structural molecules that have roles in protein synthesis; however, these RNAs are not themselves translated.

Then the spliceosme connects the 3′ end of the first exon to the 5′ end of the following exon, cleaving the 3′ end of the intron in the process. While these regions may correspond to regulatory sequences, the biological significance of having many introns or having very long introns in a gene is unclear. Some of the bases of pre-rRNAs are methylated for added stability. The first step in their processing is the digestion of the RNA to release individual pre-tRNAs. The 5′ end of the pre-tRNA, called the 5′ leader sequence, is cleaved off.There are different tRNAs for the 21 different amino acids. A significant number of eukaryotic and archaeal pre-tRNAs have introns that have to be spliced out. But over 100 other modifications can occur. The 40S subunit is composed of the 18S rRNA and 33 proteins. The anticodon is a three-nucleotide sequence, unique to each different tRNA, that interacts with a messenger RNA (mRNA) codon through complementary base pairing.The two subunits join to constitute a functioning ribosome that is capable of creating proteins. The spliceosome cleaves the pre-mRNA’s sugar phosphate backbone at the G that starts the intron and then covalently attaches that G to an internal A nucleotide within the intron. An enzyme called poly (A) polymerase (PAP) is part of the same protein complex that cleaves the pre-mRNA and it immediately adds a string of approximately 200 A nucleotides, called the poly (A) tail, to the 3′ end of the just-cleaved pre-mRNA.

Splicing occurs by a sequence-specific mechanism that ensures introns will be removed and exons rejoined with the accuracy and precision of a single nucleotide. In archaea and eukaryotes, each pre-tRNA is transcribed as a separate transcript.Pre-mRNAs are first coated in RNA-stabilizing proteins; these protect the pre-mRNA from degradation while it is processed and exported out of the nucleus. Some of a ribosome’s RNA molecules are purely structural, whereas others have catalytic or binding activities.All introns in a pre-mRNA must be completely and precisely removed before protein synthesis. Multiple nucleotides in the pre-tRNA are chemically modified, altering their nitorgen bases. The DNA gene contains the code for both the exons and the introns, as does the primary RNA transcript, but the noncoding intron sequences must be removed to form the mRNA before protein synthesis.β-thalassemia, a hemoglobin disease, can be caused by an intron mutation that prevents recognition of a splice site.