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From DNA to Protein
From DNA to Protein

... F Steps d and e are repeated over and over until the ribosome encounters a stop codon in the mRNA. The mRNA transcript and the new polypeptide chain are released from the ribosome. The two ribosomal subunits separate from each other. Translation is now complete. Either the chain will join the pool o ...
Word file (37 KB )
Word file (37 KB )

... took one sample out and used the remaining 77 samples to define a classifier based on the set of 231 discriminating genes. Then we predicted the outcome of the one sample we left out in the first place. The prediction of the left out sample is based on its correlation coefficient to the “good progno ...
relates Mendel`s discoveries to actual behavior of chromosomes
relates Mendel`s discoveries to actual behavior of chromosomes

... A. Wild Type- the normal phenotype for a character (such as red eyes in a fruit fly) B. Mutant Phenotype- a trait that is alternative tot he wild type (such as white eyes) C. Sex-Linked Genes- genes (such as eye color for fruit flies) that are located exclusively on one’s X chromosome, with no corre ...
Mendel and Heredity
Mendel and Heredity

... About 99.9% of everyone’s DNA is identical. But look around you and you’ll see a huge variety of traits such as eye color, hair color and texture, height and weight. Mendel’s peas are a good place to start learning about genetics. But the great variety in living things is not just a result of domina ...
Cloning Disease Genes in the Human Genome
Cloning Disease Genes in the Human Genome

... Cloning a gene is only the first step in finding therapies for disorders. Once a gene  has been identified and cloned, if the gene does not have a known function then  its function has to be determined before any clinical benefits besides diagnostic  testing can be seen. This will likely take longer ...
o How is covariation used in RNA structure
o How is covariation used in RNA structure

... b. ____ The process by which information in RNA is used to make proteins is called translation. c. ____ The process in which information in DNA is copied into RNA is called transcription. d. ____ Peptide bonds are both planar and flexible. e. ____ Enzymes that catalyze reactions in the cell are alwa ...
slg mock midterm – for practice only
slg mock midterm – for practice only

... b. Each strand of both daughter molecules contains a mixture of old and newly synthesized DNA. c. The two strands of the parental molecule separate, and each functions as a template for synthesis of a new, complementary strand. d. DNA Polymerase III carries out synthesis by extending from the RNA pr ...
Chromosomal Basis of Inheritance
Chromosomal Basis of Inheritance

... He got this ratio, however, all of the white eyed flies were MALE. Therefore, the eye color trait appeared to be linked to sex. ...
E. coli DNA Gyrase Cleavage Assay Kit
E. coli DNA Gyrase Cleavage Assay Kit

... E. coli DNA gyrase is prepared from the overproducing strains JMtacA and JMtacB (Hallett et al., 1990) and is supplied as an A2B2 complex. The enzyme is supplied at a concentration of 2.0 μM in Dilution Buffer and is suitable for cleavage assays. Cleavage activity is 2 U/μl. 50 % cleavage can be obt ...
Human Chromosomes
Human Chromosomes

...  Half of all sperm cells carry an X chromosome and half carry the Y.  This ensures that about half of the zygotes will be female XX and half will be male XY. ...
Biology 520 Second Sem exam
Biology 520 Second Sem exam

... chromosome theory of inheritance nondisjunction ...
Glencoe Biology - Leon County Schools
Glencoe Biology - Leon County Schools

...  Consist of a five-carbon sugar, a phosphate group, and a nitrogenous base ...
Mendelian genetics complete
Mendelian genetics complete

...  F2 generation – Offspring produced from _F1 x F1________. In F2, trait that disappeared in F1 reappeared in __1/4___ of the offspring; the other ¾ showed _dominant trait_____. C. Mendel’s Principles – After analyzing his results carefully, Mendel formed conclusions that increased understanding of ...
Newsletter Spring 2012 TRANSFAC® / ExPlain
Newsletter Spring 2012 TRANSFAC® / ExPlain

... tools for further analysis. For example, import the list of associated genes into the Ontology Search tool in order to identify overrepresented functions associated with the genes potentially regulated by the transcription factor. Or import the list of associated genes, or the FASTA sequences for th ...
Topic 4.3: Theoretical genetics
Topic 4.3: Theoretical genetics

... • Genes carried on the sex chromosome ▫ Because the Y chromosome is significantly smaller than the X chromosome, it has fewer loci and therefore fewer genes than the X chromosome  This means that sometimes alleles present on the X chromosome have nothing to pair up with.  For example, a gene whose ...
Genetic Disorders and Genetic Testing
Genetic Disorders and Genetic Testing

...  In this activity, you will assume the role of a genetic counselor and meet with clients faced with difficult decisions regarding genetic disorders and genetic testing.  Your goal is to effectively explain the disease or disorder to your clients as well as to outline potential options for genetic ...
Mendel`s First Law of Genetics (Law of Segregation)
Mendel`s First Law of Genetics (Law of Segregation)

... Mendel's First Law of Genetics (Law of Segregation) • Mendel was able to demonstrate that traits were passed from each parent to their offspring through the inheritance of genes. • Mendel's experimental organism was a common garden pea (Pisum sativum), which has a flower that lends itself to selfpol ...
Answers to most Study Problems for Quiz 1
Answers to most Study Problems for Quiz 1

... 6. a. The ratio of wildtype to mutant was 15:1 rather than the 3:1 ratio expected from a single gene trait. A = wt a = loss-of-function mutation B= wt b = loss-of-function mutation A-B- wildtype aaB- wildtype A-bb wildtype aabb = piggy b. Hypothesis: piggy is a single gene trait with 2 alleles that ...
lec03-1
lec03-1

... The promoters tell the polymerase where to start. However, there are other sequences that affect the rate of transcription. Enhancers and Silencers: In eukaryotic cells there are sequences that influence the rate of transcription by interaction with specific proteins. Sequences that increase the rat ...
Nerve activates contraction - Green River Community College
Nerve activates contraction - Green River Community College

Identification of porcine Lhx3 and SF1 as candidate genes for QTL
Identification of porcine Lhx3 and SF1 as candidate genes for QTL

... in this region, and may conceivably play roles in processes affected by the QTL. In addition, a group of tumour necrosis factor (TNF) associated protein genes (TRAF1, TRAF2 and TNFSF8) lie in this region, although the primary roles for these proteins are related to maturation and activation of blood ...
Molecular Genetics - Mrs. Mattheus Science
Molecular Genetics - Mrs. Mattheus Science

...  Consist of a five-carbon sugar, a phosphate group, and a nitrogenous base ...
*Exam3 2015 key Revised
*Exam3 2015 key Revised

... B) E. coli chromosome. C) messenger RNA. D) plasmid. E) yeast “ARS” sequence. Circle the correct answer. 34. [2 points] The PCR reaction mixture does not include: A) oligonucleotide primer(s). B) all four deoxynucleoside triphosphates. C) DNA containing the sequence to be amplified. D) DNA ligase. E ...
Synthetic approaches to transcription factor
Synthetic approaches to transcription factor

... transcription factor regulation and function Tim Johnstone BIOL1220 Spring 2010 ...
11-2Probability and PunneTt Squares
11-2Probability and PunneTt Squares

... Heterozygous- Organisms that have two different alleles for the same trait  organisms are hybrid for a particular trait.  One allele for black fur and one allele for white fur ...
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Gene



A gene is a locus (or region) of DNA that encodes a functional RNA or protein product, and is the molecular unit of heredity. The transmission of genes to an organism's offspring is the basis of the inheritance of phenotypic traits. Most biological traits are under the influence of polygenes (many different genes) as well as the gene–environment interactions. Some genetic traits are instantly visible, such as eye colour or number of limbs, and some are not, such as blood type, risk for specific diseases, or the thousands of basic biochemical processes that comprise life.Genes can acquire mutations in their sequence, leading to different variants, known as alleles, in the population. These alleles encode slightly different versions of a protein, which cause different phenotype traits. Colloquial usage of the term ""having a gene"" (e.g., ""good genes,"" ""hair colour gene"") typically refers to having a different allele of the gene. Genes evolve due to natural selection or survival of the fittest of the alleles.The concept of a gene continues to be refined as new phenomena are discovered. For example, regulatory regions of a gene can be far removed from its coding regions, and coding regions can be split into several exons. Some viruses store their genome in RNA instead of DNA and some gene products are functional non-coding RNAs. Therefore, a broad, modern working definition of a gene is any discrete locus of heritable, genomic sequence which affect an organism's traits by being expressed as a functional product or by regulation of gene expression.
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