Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Mutation silent

Mutations Point mutations silent, missense, nonsense Frameshift (delete 1 or 2 nudeotides not multiple of 3) Large segment deletion ... [Pg.61]

Types of mutations Silent means protein product not affected missense means single amino acid substitution leading to significant alteration (snch as sickle cell) and nonsense means that a stop codon is formed. [Pg.122]

Know the definitions of point mutations (silent, missense, and nonsense), insertions, deletions, and frameshift mutations. [Pg.122]

Synonymous mutation (silent mutation) a base substitution resulting in a codon that codes for the same amino acid... [Pg.47]

Many strains of Streptomyces peucetius produce daunomydn. These strains often cany a permanently repressed (silent) gene that codes for the enzyme duanomycin 14-hydroxylase. If this is reactivated by mutation, the daunomycin is further metabolised to produce a new antibiotics, 14-hydroxydaunomydn (adnamydn). [Pg.182]

There may be no detectable effect because of the degeneracy of the code. This would be more likely if the changed base in the mRNA molecule were to be at the third nucleotide of a codon such mutations are often referred to as silent mutations. Because of wobble, the translation of a codon is least sensitive to a change at the third position. [Pg.361]

Mutations are either exonic or intronic. Missense, deletion and silent mutations are found in the coding region, with intronic mutations being located close to the splice-donor site of the intron following the alternatively... [Pg.754]

A base substitution can also result in the formation of a new inappropriate terminator (or non-sense) codon, and are thus known as non-sense mutations. The polypeptide formed from such mutated genes will be shorter than normal and is most likely to be inactive. Owing to the redundancy of the genetic code, about a quarter of all possible base substitutions will not result in an amino acid replacement and will be silent mutations. [Pg.183]

Subject variability High intraindividual variability in QTc values (circadian and seasonal variation law of regression to the mean) High interindividual variability in QTc values (males versus females) Unknown prevalence in the general population of subjects carrying silent mutations in the ion channels responsible for cardiac repolarization (these subjects have normal QTc value but reduced repolarization reserve) Variability in the individual metabolic capacity for a given drug... [Pg.73]

Molecular phylogeny is a discipline that studies species differences between DNA or protein sequences. Its basic tenet is that during evolution, the sequences have drifted apart by mutation and selection as well as by random drift and fixation of variants in certain positions. The earlier two species separated the more differences became fixed. Phylogenetic trees are constructed on the basis of mutual differences of protein and/or DNA sequence. Comparison of intraspecies variation with between-species variation may in the future yield information on the neutralist/selectionist alternative. McDonald and Kreitman (1991) devised an interesting test against neutrality that compared the ratio of silent/replacement mutation of a given locus within a species with the same ratio between two related species. Under the neutral theory this should be equal (corrected for sample size), but in fact it is not (see Li, 1997, and Hudson, 1993, for a discussion). [Pg.415]

After completing the reaction, only those double-stranded vectors containing a mutation should be present. However, this is not always the case as the process is never 100( efficient. One way to rapidly screen the final product of mutants is to build a silent unique restriction site into the primer along with the required... [Pg.433]

The ability to alter gene expression spatially and temporally in the adult mouse is normally achieved by interbreeding different GEMMs with the aim to merge different genetic modifications in the same mouse. In general, one allele consists of a silent mutation that will only be induced when the inductor is expressed and activated in a tissue-specific, inducible, or temporal manner (Figs, lb, e and 2). [Pg.286]


See other pages where Mutation silent is mentioned: [Pg.110]    [Pg.262]    [Pg.110]    [Pg.262]    [Pg.229]    [Pg.140]    [Pg.1385]    [Pg.256]    [Pg.298]    [Pg.65]    [Pg.168]    [Pg.169]    [Pg.273]    [Pg.752]    [Pg.48]    [Pg.60]    [Pg.148]    [Pg.12]    [Pg.58]    [Pg.89]    [Pg.66]    [Pg.66]    [Pg.234]    [Pg.417]    [Pg.427]    [Pg.388]    [Pg.198]    [Pg.433]    [Pg.434]    [Pg.437]    [Pg.46]    [Pg.52]    [Pg.186]    [Pg.301]    [Pg.357]    [Pg.68]    [Pg.133]    [Pg.134]    [Pg.285]   
See also in sourсe #XX -- [ Pg.361 ]

See also in sourсe #XX -- [ Pg.332 , Pg.357 ]




SEARCH



SILENT

© 2024 chempedia.info