DNA helicase unwinds double-stranded DNA into single strands during replication by separating the strands at the replication fork, which is created by the helicase and consists of a leading and lagging strand. DNA ligase joins DNA strands by catalyzing phosphodiester bond formation, while DNA polymerase synthesizes new DNA strands using deoxynucleotides as building blocks. Okazaki fragments on the lagging strand are synthesized discontinuously and later joined by ligase. Introns in RNA transcripts are removed by splicing in the nucleus, with exons being joined together and introns discarded.
DNA helicase unwinds double-stranded DNA into single strands during replication by separating the strands at the replication fork, which is created by the helicase and consists of a leading and lagging strand. DNA ligase joins DNA strands by catalyzing phosphodiester bond formation, while DNA polymerase synthesizes new DNA strands using deoxynucleotides as building blocks. Okazaki fragments on the lagging strand are synthesized discontinuously and later joined by ligase. Introns in RNA transcripts are removed by splicing in the nucleus, with exons being joined together and introns discarded.
DNA helicase unwinds double-stranded DNA into single strands during replication by separating the strands at the replication fork, which is created by the helicase and consists of a leading and lagging strand. DNA ligase joins DNA strands by catalyzing phosphodiester bond formation, while DNA polymerase synthesizes new DNA strands using deoxynucleotides as building blocks. Okazaki fragments on the lagging strand are synthesized discontinuously and later joined by ligase. Introns in RNA transcripts are removed by splicing in the nucleus, with exons being joined together and introns discarded.
DNA helicase unwinds double-stranded DNA into single strands during replication by separating the strands at the replication fork, which is created by the helicase and consists of a leading and lagging strand. DNA ligase joins DNA strands by catalyzing phosphodiester bond formation, while DNA polymerase synthesizes new DNA strands using deoxynucleotides as building blocks. Okazaki fragments on the lagging strand are synthesized discontinuously and later joined by ligase. Introns in RNA transcripts are removed by splicing in the nucleus, with exons being joined together and introns discarded.
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TERMS DEFINITION
DNA helicase DNA helicases are essential during DNA
replication because they separate double- stranded DNA into single strands allowing each strand to be copied. Replication fork The replication fork is a very active area where DNA replication takes place. It is created when DNA helicase unwinds the double helix structure of the DNA. The replication fork looks like a fork in the road that is composed of a leading strand and a lagging strand of DNA. Leading strand Parent strand. 3’ is free end. 5’ nearest to replication fork. upstream Lagging strand Parent strand. 5’ free end. 3’ nearest to replication fork. Downstream DNA ligase DNA ligase is a specific type of enzyme, a ligase, that facilitates the joining of DNA strands together by catalyzing the formation of a phosphodiester bond. DNA polymerase DNA polymerase is an enzyme that synthesizes DNA molecules from deoxyribonucleotides, the building blocks of DNA. These enzymes are essential for DNA replication and usually work in pairs to create two identical DNA strands from a single original DNA molecule. TATA box In molecular biology, the TATA box is a sequence of DNA found in the core promoter region of genes in archaea and eukaryotes. Pribnobox - prokaryotes A TATA box is a DNA sequence that indicates where a genetic sequence can be read and decoded. It is a type of promoter sequence, which specifies to other molecules where transcription begins. Okazaki Fragments Okazaki fragments are short sequences of DNA nucleotides (approximately 150 to 200 base pairs long in eukaryotes) which are synthesized discontinuously and later linked together by the enzyme DNA ligase to create the lagging strand during DNA replication. tRNA Transfer ribonucleic acid (tRNA) is a type of RNA molecule that helps decode a messenger RNA (mRNA) sequence into a protein. tRNAs function at specific sites in the ribosome during translation, which is a process that synthesizes a protein from an mRNA molecule. rRNA Ribosomal ribonucleic acid (rRNA) is a noncoding Francis
type of RNA that acts as the primary building
block for ribosomes and the assembly line on which protein synthesis occurs in those ribosomes, essential to all living organisms. Anticodon An anticodon is a trinucleotide sequence complementary to that of a corresponding codon in a messenger RNA (mRNA) sequence. An anticodon is found at one end of a transfer RNA (tRNA) molecule. codon A codon is a sequence of three DNA or RNA nucleotides that corresponds with a specific amino acid or stop signal during protein synthesis. DNA and RNA molecules are written in a language of four nucleotides; meanwhile, the language of proteins includes 20 amino acids. Polypeptide Chain Polypeptide chains are polymers of amino acids joined together with peptide bonds. These peptide bonds are formed through condensation reactions whilst the amino acids are being coded for during translation. Whilst in polypeptide chains, amino acids are known as residues. RNA primase Primase is an enzyme that synthesizes short RNA sequences called primers. These primers serve as a starting point for DNA synthesis. Since primase produces RNA molecules, the enzyme is a type of RNA polymerase. RNA polymerase RNA polymerase, abbreviated RNAP or RNApol, officially DNA-directed RNA polymerase, is an enzyme that synthesizes RNA from a DNA template. RNAP locally opens the double- stranded DNA so that one strand of the exposed nucleotides can be used as a template for the synthesis of RNA, a process called transcription. Termination signal A termination signal is found at the end of the part of the chromosome being transcribed during transcription of mRNA. It is needed because only parts of the chromosome are transcribed. The beginning part is started at the promoter and then ended at the termination signal. 5’ cap and 3’ poly a tail A 5' cap is added to the beginning of the RNA transcript, and a 3' poly-A tail is added to the end. Splicing In splicing, some sections of the RNA transcript (introns) are removed, and the remaining sections (exons) are stuck back together. Spliceosome A spliceosome is a large and complex molecular machine found primarily within the nucleus of Francis
eukaryotic cells. The spliceosome is assembled
from small nuclear RNAs (snRNA) and approximately 80 proteins. The spliceosome removes introns from a transcribed pre-mRNA, a type of primary transcript. Introns An intron is any nucleotide sequence within a gene that is removed by RNA splicing during maturation of the final RNA product. In other words, Introns are noncoding regions of an RNA transcript, or the DNA encoding it, which are eliminated by splicing before translation. Exons An exon is any part of a gene that will encode a part of the final mature RNA produced by that gene after introns have been removed by RNA splicing. The term exon refers to both the DNA sequence within a gene and to the corresponding sequence in RNA transcripts. Francis