Mol Bio Flashcards
TATA box
Promoter region the binds transcription factors and RNA pol II during the initiation of transcription. Located about 25 bases upstream from the beginning of the coding region
Homeobox genes
encode DNA-binding transcription factors that play an important role in the segmental organization of the embryo along the cranio-caudal axis
- highly conserved 180 nucleotide sequence
- mutations often result in skeletal malformations and improperly positioned limbs
Mitochondrial diseases
- exclusively maternal inheritance
- variable severity of disease is explained the the random distribution of normal and mutated mitochondria btwn daughter cells during mitosis; some cells may be healthy, while other may be affected by genetic mutation (heteroplasmy)
Ex:
- Leber hereditary optic neuropathy- bilateral vision loss
- Myoclonic epilepsy with ragged-red fibers- Myoclonic seizures and myopathy assoc w exercise
- Mitochondiral encephalopathy w lactic acidosis and stroke like episodes (MELAS)
DiGeorge Syndrome
Neural crest failed migration of the 3rd(inferior parathyroid and thymus) and 4th (superior parathyroid) pharyngeal/bronchial pouches. Parathyroid and thymus hypoplasia results in T cell def.
- 22q11.2 micro deletion
- PTH def leads to hypocalcemia ->increased neuromuscular excitability, tetany, carpopedal spasms or seizures.
- tapping facial nerve elicits twitching of nose and lips (Chevostek Sign)
- absent thymic shadow
- involvement of the 2nd pouch -> short palpebral fissures, micrognathia, bifid uvula, cleft palate
Kinesin
Microtubule assoc, ATP powered motor protein that facilitates the anterograde transport of neurotransmitter-containing secretory vesicles down axons toward synaptic vesicles
Vs
Dyesin: retrograde transport, toward cell body
Langerhans cells
Form of dendritic cell most commonly found in the skin and mucous membrane; professional APC cells (interact w T cells)
Most effective form of APC
Derived from myeloid cell line
“Raquet shaped” intracytoplasmic granule -> Birebeck granules
Congenital complications of CMV infection
Chorioretinitis ***most common Sensorineural deafness Seizures Jaundice Hepatosplenomegaly Microcephaly
Ubiquitin
Protein that undergoes ATP-dependent attachment to other proteins, labeling them for degradation. Enter proteosome and are degraded into small peptides. Impairment can lead to the development of neuro degenerative disorders, including Parkinson’s and Alzheimer’s
Primase
DNA dependent RNA polymerase that incorporates short RNA primers into replicating DNA
Linkage disequilibrium
2 genetic loci are said to be in linkage disequilibrium when their respective alleles are inherited together in the same gamete more or less often than expected by chance alone. Often the result of physical proximity of genes on the same chromosome
–> genes in close proximity become linked
Heteroplasmy
Presence of different Mitochondiral genomes (i.e. Mutated and wild type) within a single cell. Severity of mitochondrial diseases often related to the portion of abnormal mitochondria
Pleiotropy
Occurrence f multiple phenotypic manifestations, often in different organ systems, which result from mutation in a single gene