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Name:
Name:

... Get it? Good. Let’s take a test!  OK…maybe you’re as confused as I would ...
Common Assessment Review
Common Assessment Review

... gamete formation. Genes on separate chromosomes sort independently during meiosis. Each allele combination is equally likely to occur. Law of Segregation- Two alleles for each trait separate during meiosis. During fertilization, two alleles for that trait unite. ...
CA Update from Dr. Beever 07-26-2010
CA Update from Dr. Beever 07-26-2010

... early 2009, a number of US breeders provided samples of affected calves that from pedigree information also demonstrated recessive inheritance and implicated the same common ancestor as in Australia. This was further established by using DNA from affected calves to map the gene responsible to a uniq ...
Variation and selection
Variation and selection

... 1. This is where individuals fall into a number of distinct classes or categories, and is based on features that cannot be measured across a complete range. 2. There are no intermediates between categories. 3. You either have the characteristic or you don't. ...
Mechanisms of Evolution
Mechanisms of Evolution

... • Third position mutations often silent (synonymous) ...
6.1 Mutation
6.1 Mutation

... More Variation Examples ...
Regulation and mutation
Regulation and mutation

... RNA processing: different exons may be used within one gene, producing different protein products mRNA longevity: mRNA translates as long as it is intact ‘lifespan’ encoded in the 3' UTR sequence AUUUA signals early degradation translation: ...
Biol 3301: Genetics Exam #3 Practice questions
Biol 3301: Genetics Exam #3 Practice questions

... a) A double strand DNA circle b) A retrovirus c) Double-strand RNA d) Single-strand RNA e) Single-strand DNA 27. (3) What protein does a P-element transposon encode and what is the function of this protein? It encodes transposase, which interacts with the inverted repeats at the termini of the ...
Lecture # 5 Mutations
Lecture # 5 Mutations

... There are genetic tests available for many of the human genetic disorders. DNA, RNA, chromosomes or proteins may be analyzed in order to make the diagnosis. Testing may be done for a variety of reasons, such as in order to determine if an individual carries a defective gene that runs in their family ...
Viruses as Pathogens in Bacterial Gene Regulation
Viruses as Pathogens in Bacterial Gene Regulation

... – benefit: single on & off switch for entire process • switch is called the operator – located within the promoter region – can be switched off by the presence of a repressor bound to the operator » blocks attachment of the RNA Pol » product of a repressor gene that is some distance from the operon ...
Honors Biology
Honors Biology

... 1. Protein Synthesis  base triplets/codons/anticodons: what are they?, what type of information do they represent?, to what molecules do these terms refer to?  redundancy of the DNA code: what advantage does having multiple codons for a single amino acid give when a mutation occurs?  amino acid s ...
DNA powerpoint
DNA powerpoint

... order. Then it goes back out to pick up some more (like a taxi cab picking up more people to bring to the location) • The amino acids get strung along into a “necklace” and when it is complete you have a protein ...
Exam 2 Key v3 Bio200 Win16
Exam 2 Key v3 Bio200 Win16

... 5/ 3a) Short chromosomes are copied well. Longer chromosomes are either delayed, or the interior regions of the DNA are never completely replicated. _____ Synonymous mutation in the gene encoding the helicase enzyme _____ Mutation in the promoter regions of all genes encoding DNA polymerase enzymes ...
The Universal Genetic Code - Willimon-PHS
The Universal Genetic Code - Willimon-PHS

... • The sides of one DNA molecule is connected with bonds between the phosphate group and the deoxyribose sugar • The two DNA strands connect by bonds between nitrogenous bases o A always bonds with T o G always bonds with C Role of DNA DNA is the genetic material of organisms. • Information coded in ...
Inheritance Poster 1
Inheritance Poster 1

... another or show a striking difference to one another, e.g. tall and dwarf, yellow and green, etc. DNA: substance found in cell nuclei in the chromosomes. Regulates protein synthesis and is the main molecule of genes. DNA profile: a picture (auto radiograph) of the pieces of DNA produced when an orga ...
Jennifer Kallini - Adrenoleukodystrophy
Jennifer Kallini - Adrenoleukodystrophy

... Maoris ...
genetic basis of congenital heart disease and molecular
genetic basis of congenital heart disease and molecular

Protein Malfunction and Disease: Making a Sickle Cell Mutation
Protein Malfunction and Disease: Making a Sickle Cell Mutation

... The result of the mutation is a misshaped protein that includes a replacement of a hydrophilic glutamic acid (E) for hydrophobic valine (V). In this activity you will look at the amino acid change and determine the molecular basis for the disease that lies in the DNA. You will then be asked to relat ...
PCR-assay of intragenic DNA lesions induced by ionizing radiation
PCR-assay of intragenic DNA lesions induced by ionizing radiation

... observed; To detect the intragenic distribution of different DNA alterations relative to the exon-intron structure of the gene under study ...
4.2.08 105 lecture
4.2.08 105 lecture

... transcription unit - the part of a gene that gets copied (transcribed) by RNA polymerase coding region – For genes that make (encode) proteins, the coding region is part of the transcription unit. The coding region is the genetic information in the DNA that tells the specific structure (primary ami ...
2nd Nine Weeks Exam Review Unit 5
2nd Nine Weeks Exam Review Unit 5

... D. No change in amino acids would occur. DNA can be changed by UV radiation. If the sun damages skin cells what is most likely to occur? A. A somatic mutation that will not affect offspring. B. A somatic mutation that could also affect the offspring. C. A germ cell mutation with no effect on the ind ...
Mutations - Warren County Schools
Mutations - Warren County Schools

... chloride ion channel in cell membranes. Abnormal CFTR cannot be transported to the cell membrane. ...
Sections 3 and 4 ANSWERS
Sections 3 and 4 ANSWERS

... – Point where one nitrogen base is substituted for another – Sickle Cell Anemia: substitute A for T ...
Hydrophobic: tending to repel and not absorb water
Hydrophobic: tending to repel and not absorb water

... Hydrophobic: tending to repel and not absorb water; tending not to dissolve in or mix or be wetted by water. ...
Document
Document

... Objective: To know the major steps in protein synthesis and the RNAs and proteins involved in this process. To understand the mechanism by which proteins are targeted to specific cimpartments. I. Genetic code A. Three nucleotides make one codon B. "Universal" C. Degenerate D. Commaless II. Translati ...
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Point mutation



A point mutation, or single base modification, is a type of mutation that causes a single nucleotide base change, insertion, or deletion of the genetic material, DNA or RNA. The term frameshift mutation indicates the addition or deletion of a base pair. A point mutant is an individual that is affected by a point mutation.Repeat induced point mutations are recurring point mutations, discussed below.
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