On the complementarystrand Sicklecell anemia Insertion One or more extra nucleotides areinserted into replicating DNA, often resulting in a frameshift One form of beta thalassemia Deletion OneDNA Mutation and Repair A mutation, which may arise during replication and/or recombination, is a permanent change in the nucleotide sequence of DNA Damaged DNA can be mutated either byThis mutation is linked to sicklecell anemia Insertion one or more extra nucleotides are inserted into replicating DNA, often resulting in a frameshift Linked to one form of betathalassemia
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One or more extra nucleotides are inserted into replicating dna often resulting in a frameshift
One or more extra nucleotides are inserted into replicating dna often resulting in a frameshift- Genes are segments of DNA located on chromosomes A gene mutation is defined as an alteration in the sequence of nucleotides in DNA This change can affect a single nucleotideDNA Repair DNA polymerase can make mistakes while adding nucleotides It edits the DNA by proofreading every newly added base Incorrect bases are removed and replaced by the correct



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NCERT Solutions NCERT Solutions For Class 12 More NCERT Solutions for Class 10 Science NCERT SolutionsDNA replication is called semiconservative because the two resulting DNA molecules each have one new DNA strand and one old strand from the original DNA molecule both of the resultingEukaryotic genomes are much more complex and larger than prokaryotic genomes and are typically composed of multiple linear chromosomes ( Table 112 ) The human genome, for example, has 3
Here, the chromosomes swap one or more gene(s) with another chromosome (Slide 14) A nondisjunction mutation does not involve any errors in DNA replication or crossingoverCourse Title HUM 723;Frameshift mutations occur most often because one or more nucleotides are either inserted, or deleted from DNA The result can be a completely new sequence of codons and nonfunctional
Find an answer to your question Substitutions, additions, or deletions of one or more nucleotides in the DNA molecule are called _____ a Genetic variat Shelseyman ShelseymanRepair enzymes bind to damaged DNA repair enzymes excise the damaged DNA and some surrounding bases DNApolymerase synthesizes the correct nucleotides DNA ligase seals the sugarphosphate backboneThe two resulting DNA molecules each have one new DNA strand and one old strand from the original DNA molecule Both of the resulting DNA molecules are composed of new strands of



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Insertions add one or more extra nucleotides into the DNA They are usually Insertions add one or more extra nucleotides into the School San Francisco State University; A nucleotide is the basic building block of nucleic acids (RNA and DNA) A nucleotide consists of a sugar molecule (either ribose in RNA or deoxyribose in DNA) attached to aHot spots include areas of the genome with highly repetitive sequences, such as trinucleotide repeats, in which a sequence of three nucleotides is repeated many times During DNA



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So these end times are essential for the DNA replication And usually works in the groups to create the two identical They are in a duplex from a single original DNA So this is responsible for the DNA polymerases are able to add nucleotides at very impressive rates In the bacteria E coli, new strands of DNA are built at a rate of around 500 new nucleotides per second Human Frameshift mutations are insertions or deletions in the genome that are not in multiples of three nucleotides They are a subset of insertiondeletion (indel) mutations that are



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One or more extra nucleotides are inserted into replicating DNA, often resulting in a frameshift c) Deletion One or more nucleotides is "skipped" during replication or otherwiseAs a result, during DNA replication, DNA polymerase may either skip replicating several nucleotides (creating a deletion) or insert extra nucleotides (creating an insertion) EitherDescribe the structure of DNA is a double helix composed of two complementary strands of nucleotides The sides are composed of phosphate and sugar, and the steps are composed of



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One or more extra nucleotides are inserted into replicating DNA, often resulting in a frameshift One form of betathalassemia Deletion One or more nucleotides is "skipped"During proofreading, DNA polymerase enzymes recognize this and replace the incorrectly inserted nucleotide so that replication can continue Proofreading fixes about 99% of these types ofSometimes lesions may cause bases to be skipped during replication or cause extra nucleotides to be inserted into the backbone DNA polymerases can also slip during the replication of regions of



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Many mutations are point mutations that replace one nucleotide with another;Answer (1 of 2) The dangers of any mutation usually include * An abnormally transcribed DNA sequence (mRNA) * Resulting abnormal translated protein * An abnormal or lethal phenotype Insertions are mutations in which extra base pairs are inserted into a new place in the DNA The number of base pairs inserted can range from one to thousands!



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DNA Replication Steps/Stages Initiation This is the stage where DNA replication is initiated DNA synthesis is initiated within the template strand at a specific coding region site Gene duplication refers to a mutation during which a sequence of genetic information is duplicated These mutations contrast to deletions, translation, and transversion mutations Molecular Biology DNA synthesis (Replication) 1) In most organisms, DNA is a genetic material that stores the information template for the synthesis of RNA and subsequently



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Insertion An insertion changes the DNA sequence by adding one or more nucleotides to the gene As a result, the protein made from the gene may not function properly Deletion A deletion A deletioninsertion (delins) variant may also be known as an insertiondeletion (indel) variant Duplication A duplication occurs when a stretch of one or more nucleotides in a gene isGet the detailed answer 8) Nucleotides contain one or more phosphate groups that are usually attached to the 1) C3' or C5' atoms 2) C3 or N5 atoms 3) non



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Insertion (genetics) In genetics, an insertion (also called an insertion mutation) is the addition of one or more nucleotide base pairs into a DNA sequence This can often happen in microsatelliteOne or more extra nucleotides are inserted into replicating DNA, often resulting in a frameshift One form of betathalassemia Deletion One or more nucleotides is "skipped" during replication orBoth of the resulting DNA molecules are composed of new strands of nucleotides no extra nucleotides are incorporated into the replicated DNA molecules the sequence of nucleotides in



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In proof reading during DNA replication Login Study Materials BYJU'S Answer;VIDEO ANSWERHello So let's answer now the question let's fill in the blanks Okay so the D N A Is a biological molecule found in the um the next the first answer is we have the nucleus So it isTranscribed image text of one or more Frameshift mutations are caused by the nucleotides in DNA a) chemical modification Ob) deletion c) insertion d) A and C e) B and C The image below



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Get the detailed answer during dna replication how many nucleotides are copied per second Get the detailed answer during dna replication how many nucleotides are copied per second 🏷️An insertion occurs when an extra nucleotide is incorporated into the DNA sequence during replication A deletion mutation occurs when a nucleotide is skipped or absent from the A frameshift mutation is an insertion or deletion mutation that affects the reading frame of the gene, resulting in large numbers of altered amino acids Inserting or deleting



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Often, the more the repeats, the less the activity of the gene involved They occur in some human diseases such as Huntington's disease and fragileX syndrome Normal protein function DNA has directionality that can run either 3′5′ or 5′3′ based off of the carbons in the sugar group The two strands of DNA in the double helix must run opposite to each other in an antiparallel fashion Therefore, if the first strand starts at the 3′ end and finishes at the 5′ end, then the second strand must run opposite, starting at the 5′ end and finishing at the 3′ endOthers involve insertion or deletion of one or a few nucleotides Mutations result either from errors in DNA



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Insertions add one or more extra nucleotides into the DNA They are usually caused by transposable elements , or errors during replication of repeating elements Insertions in theThree nucleotide pairs are inserted into DNA expanding nucleotide repeat Mutation in which the number of copies of a set of nucleotides (most often three nucleotides) increases in succeedingPoint Mutation Type of mutation in DNA or RNA, the cell's genetic material, in which one single nucleotide base is added, deleted or changed, Chromosomal Mutation Occurs as a result of



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