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61 Cards in this Set

  • Front
  • Back

Asexual

One parent makes genetically identical offspring



Chromatin

DNA + Proteins

Interphase

-G1


-S


-G2




During this phase, the entire chromosome is copied and the two identical copies are connected to the centromere

M Phase

Mitosis


Goes through Prophase, Metaphase, Anaphase, and Telephase





Sister Chromatids

Two identical copies of a chromosome

Contact Inhibition

Stops dividing when comes into contact of another cell

Anchorage Dependence

Divide only when attached



Benign Tumors

Noncancerous; and does not affect the surrounding structures



Malignant Tumors

Cancerous; Invade surrounding structures and cause metastasis



Metastasis

Break away and start new cancers elsewhere



Crossing-Over

Recombines genes on sister chromosomes of homologous pairs

Independent Assortment of Chromosomes

Gametes have all the possible chromosome combinations

Random Fertilization

Every egg and sperm carry different chromosome combinations and its random which two meet

Gene

The basic unit of hereditary



Allele

Alternate forms of a gene

Dominant Allele

Will be seen if present

Recessive Allele

Will only be seen if the dominant is not present

Phenotype

Refers to an individual's physical appearance



Genotype

Refers to an individual's alleles



Homozygous

Same alleles



Heterzygous

Two different alleles

Autosomal Recessive Disorders

Recessive disorders that are passed on by parents who are unaffected

Autosome Dominant Disorders

Dominant disorders are passed on by a parent who has, or will develop the disorder



Codominance

When alleles are equally expressed in a heterozygote

Incomplete Dominance

Intermediate phenotype

Pleiotrophy

One gene influences many traits

Epistasis

An allele of one gene mask the expression of alleles at a different gene and the ratio deviates from expected ratio

Expressivity

Range of phenotypes expressed by 1 genotype under different environmental conditions

Multifactorial

Have a genetic component and environmental component

Pedigree

Chart showing the genetic connections among individuals

Dosage compensation

In females, only one X chromosome is active, other is condensed into Barr body

Aneuploidy

1 missing or extra chromosome

Nondisjunction

Failure of one pair of homologous chromosomes to seperate

XXX

Females with an extra chromosome; Meta female

XYY

Males with an extra Y chromosome; Jacobs Syndrome

XXY

Males with an extra X chromosome; Klinefelter syndrome

XO

Females with one chromosome; Turner syndrome

Genomic Imprinting

Expression of a gene in a given tissue or developmental stage is based on whether the gene was inherited from the male or female parent

Polyploidy

Presence of multiple sets of chromosomes

Genome

Complete set chromosomes

Chromosomes

Carriers of DNA

DNA

Genetic Material

Gene

Portion of DNA with instructions to make protein

Allele

Alternate versions of a gene that code for the same trait

Nucleotides

Sugar, Phosphate, and base

Semiconservative Replication

Each parental strand serves as a template for one new strand

Transcription

DNA used to make RNA

Translation

RNA used to make proteins

Lagging Strand

DNA Polymerase works away from replication fork


Separate RNA primer initiates each Okazaki fragment


- Fragments joined by DNA Ligase

Nuclear Excision Repair

Repairs thymine dimers caused by the sun's UV radiation and chemicals

Telemeres

Protect genes from eroding during duplication

Transcription

RNA synthesized from DNA strand

Translation

Polypeptide synthesized of using the mRNA template

RNA

Made up of nucleotides containing the sugar ribose and the base uracil in place of thymine

Initiation

RNA Polymerase binds to promotor region unwinding and opening strands



Elongation

RNA Polymerase moves 5' -> 3' adding complementary RNA nucleotides to new RNA transcript

Termination

RNA Polymerase stops and RNA & DNA released

Modification

Capping and editing, a cap and tail are added to ensure protection and recognition

Mutations

Permanent changes in genetic material

Point Mutations

Changes in just one base pair

Frameshift

Additions or losses of nucleotide pairs in a gene