Unit 3: Flashcards
Who discovered the chemical structure of DNA?
James Watson and Francis crick
What name is given to the structure of DNA?
Deoxyribonucleic
Four nitrogenous bases in DNA:
- Thymine
- Cytosine
- Adenine
- Guanine
What is complimentary base pairing?
Nucleutoid bases linked by an H bond. Guanine and cytosine are complimentary + adenine and thymine
3 components of a nucleotide:
Sugar (deoxyribose), a phosphate, and one of four bases (thymine, cytosine, guanine, adenine)
Tay Sachs: and what is the treatment?
Caused by absence of hex-a (vital enzyme). No cure but treatments are available for symptom care. (Seizures, epilepsy, mucus buildup, physical care, feeding tubes)
PKU:
Phenylketonuria. A rare genetic condition that causes amino acid (
PKU treatment:
Special diet that limits food with phenylalanine or high protein. Babies need special formula called lofenalac.
Sickle cell anemia:
The body produces abnormally shaped red blood cells (crescent or sickle shaped). They can block blood flow and cause clotting.
Karyotype:
Representation of The number, size, shape of chromosomes in organism
What can be learned from a karyotype?
It is easy to view abnormalities in the chromosomes (trisomy, missing chromosomes, mutations) that can cause problems in growth and development
Polygenic traits:
Characteristic controlled by 2 or more genes located on different areas on different chromosomes. (Controlled by atleast 3 genes
Traits are polygenic when:
When there is A wide variation in the trait
How is a DNA fingerprint made?
Obtain cells (skin, hair, blood). DNA is extracted and purified and sequences using gel electrophoresis. (- charge is applied so proteins move towards + charge). Compared to sample
What things can be cloned?
Plants, food, animals, body parts, drug production (animal proteins). To improve certain parts of something & to regrow human parts + medicine use
Pedigree:
The recorded ancestry showing genealogy.
Four changes in chromosome structure:
Deletion, duplication, inversion, translocation
Deletion:
Mutation where part of chromosome or DNA is lost during replication
Duplication;
Duplication of a region of DNA that contains a gene
Inversion:
Chromosome rearrangement where a segment of a chromosome is reduced end to end
When does inversion occur::
When a single chromosome undergoes a breakage and rearrangement within itself
Translocation:
Chromosomal segment is moved from one position to another (within the same Or to another chromosome)
Amniocentesis:
Medical procedure where small amniotic fluid is sampled. used in prenatal diagnosis of chromosomal abnormalities. (Fetal infection and sex determination)
Ultra sound:
Medical imaging technique that uses sound waves to produce picture inside the body.