Monday, November 30, 2015

17.3-Modifying RNA notes


17.3-Modifying RNA

  • Alteration
    • The 5’ end receives a modified nucleotide 5’ cap.
    • The 3’ end gets a poly-A tail
  • Functions
    • They seem to facilitate the expert of mRNA to the cytoplasm
    • They protect mRNA from hydrolytic enzymes
    • They help ribosomes attach to the 5’ end
  • Split genes and RNA splicing
    • Introns are noncoding regions
    • Exons are eventually expressed
    • RNA splicing removes introns and joins exons
    • RNS splicing is carried out by spliceosomes
    • Spliceosomes proteins several small nuclear ribonucleoproteins (snRNPs)
  • Ribozymes
    • Catalytic RNA molecules that function as enzymes and can splice RNA
    • The discovery of ribosomes rendered obsolete the belief that all biological catalysts were proteins.
  • 3D proteins of RNA enable it to function as an enzyme
    • Form a 3D structure, base pair with itself
    • Functional groups participate in catalysis
    • Hydrogen-bond with other nucleic acid molecules
Exon shuffling may result in the evolution of new proteins

16.1- Replication

Hhmi Replication Video 

Transcription Animation

Transcription Animation with quiz. 

Thursday, November 19, 2015

Laws of Probability 14.2

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15.1 Morgan and Flies


14.4 Notes- Human Traits

Chapter 14.4- Human Traits
·         Pedigree Analysis
o   Family Pedigree- history for a particular trait and assembling this information into a family tree describing the traits of parents and children of a certain generation.
 












o   The figure above shows the pedigree of a family with a widow-peaked hairline.
o   The importance of a pedigree is to help calculate that probability of a future child.
o   Pedigrees are more serious when the alleles could cause a serious disease or disorder
·         Recessively Inherited Disorders
o   Carriers- heterozygotes may transmit the recessive allele to their offspring
o   Genetic disorders are not distributed among all group of people
o   When a disease-causing recessive allele is rare, it is relatively unlikely that two carriers of the same harmful allele will meet and mate.
o   Cystic Fibrosis- most common lethal genetic disease in the United States
o   Sickle-Cell Disease- most common inherited disorder among people of African descent
·         Dominantly Inherited Disorders-
o   Dominant alleles that cause a lethal disease are much less common than recessive alleles that have lethal effects
o   Huntington’s Disease- a degenerative disease of the nervous system, is caused by a lethal dominant allele
·         Genetic Testing
o   Avoiding simple Mendelian disorders is possible when the risk of a particular genetic disorder can be assessed before a child is conceived
o   Fetal Testing
§  Amniocentesis- tests performed in the 14th-16th week of pregnancy
§  (CVS)- physician inserts a narrow tube through the cervix into the uterus and suctions out a tiny sample of tissue
o   Newborn Screening
§  Some genetic disorders can be detected at birth simply by biochemical tests.
§  (PKU) is the most common newborn screening test.

§  Fetal and newborn screening for serious inherited diseases, tests for identifying carriers, and genetic counseling.