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DNA Sequence chains are called
Chromosomes
Which of Mendel's law was used as evidence for the fact that with garden peas, one physical unit is from the father and one is from the mother
Mendel's law of segregation
What is usually inherited in matrilineal vs patrilineal
mtDNA and Y chromosome DNA
mtDNA
mitochondrial DNA, found in the mitochondria, contains 37 genes essential for energy production, maternally passed down
Pleiotropy
when a single gene can affect multiple physical and biochemical traits
codominant
Alleles that have both affects shown in the phenotype
Gametes
haploid cell, sex cell, half the amount of chromosomes as a somatic cell
Somatic cells
any cells of the body, diploid cells, two sets of chromosomes (one from each parent)
Mendel's Law of Independent Assortment
the alleles of different genes segregate independently of one another during gamete formation, 2^n where n is the number of chromosomes
gene pool
the individual genotypes in a breeding population taken as a whole
Research on epigenetics indicates that environmental factors can cause heritable, chemical changes in the genome without changing the DNA sequences.
true
how are amino acids joined together
peptide bonds, a covalent bond
what are amino acids joined together called
protein chain
what is the shape of a DNA molecule
helix
regulatory protein
protein that controls a biological process, interacts with other molecules, binds to specific DNA sequences eg. estrogen, antibodies, cyclins
Mitosis
one cell divides into two genetically identical daughter cells, produces 2 diploid somatic cells
Meiosis
two stages of cell division, resulting in four haploid daughter cells from a single diploid parent cell, produces gametes (sex cells), chromosome number is reduced
who first demonstrated the principles of genetic inheritance
Gregor Mendel
epigenetics
the study of how environmental factors and behaviors like diet and stress can alter gene activity without changing the DNA sequence
polygenism
the theory that humans evolved from several indecent pairs of ancestors
homeotic genes
controls development of entire body structures, a mutation would be one part growing from another
what are the four DNA bases and what do they pair with?
Adenine with Thymine, Guanine bonds with Cytosine
genotype
the genetic makeup of an individual
nondisjunction
failure of chromosomes to separate during cell division, resulting in daughter cells with an abnormal number of chromosomes, most common example is down syndrome
mRNA
messenger RNA, single stranded, crucial in translation, carries genetic info from DNA to cytoplasm
how many pairs of chromosomes do humans have?
23, 22 somatic pairs and 1 gamete
Mendel's law of segregation
one allele comes from each parent for each trait, resulting in 2 alleles per trait
nucleotide
phospate, sugar and nitrogen base
haplotype
a group of alleles that are close together on a chromosome
karyotypes
complete set of chromosomes, includes autosomes and sex chromosomes
homologous chromosomes
a pair of matching chromosomes in a diploid organism
what is the different base pair that RNA has
uracil
methylation
the process of adding a methyl group to a molecule, usually stops or represses the expression of a gene
Why do the blood types of a person providing blood for a transfusion, and the person receiving the blood, have to be of a compatible ABO type?
Blood type compatibility is essential because the recipient's immune system will attack and destroy donated red blood cells if they have foreign antigens. To prevent a dangerous transfusion reaction, compatible blood is needed, where the recipient doesn't have antibodies against the donor's blood cell antigens.
Mendel's experiments with pea plants showed that crossing plants with yellow seeds with plants with green seeds produced only offspring with yellow seeds. This finding illustrates the principle of
dominance
Individuals whose blood type is A and who carry both dominant and recessive genes at this locus have a genotype of
AO
Transcription occurs mostly in the __________ and results in the __________.
cells nucleus, production of mRNA
heteroplasmic
the biological state where an individual possesses two or more different types of mitochondrial DNA
homoplasmic
nDNA same in all cells
living fossil
living counterpart to a species known from ancient times as fossils
linkage
when genes located close together on the chromosome are inherited together as a unit during meiosis
Rosalind Franklin
discovered the helix structure of DNA through X-ray diffraction
Hox genes
regulator genes, determine placement of body parts, instructions for embryonic development
genome
the complete set of genes in an individual cell
how many chemical bases is each amino acid coded for by
3
where is DNA found in the cell?
mostly in the nucleus, with a small amount in the mitochondria
gene pool
all the alleles contained within a group of interbreeding individuals
polygenic traits
characteristics influenced by two or more genes rather than a single gene
genome
the total dna sequence of an organism
What does DNA do in protein synthesis
it is the biological code for protein synthesis, serves as a template for protein production, provides code to produce structural proteins
The scientist whose work provided the foundation for later understandings of genetics was
Gregor Mendel
what are the blood types, the present antigens, and corresponding genotypes
Type A- a antigen AA AO genotype, Type B- b antigen BB BO, Typ AB- A and B antigens AB, Type O- no antigens OO, AB is universal recipient, OO is universal donor
Genotype, phenotype and allele frequency
#of individuals with a specific phenotyp/genotype / total individuals in the population #of specific allele in the population / total alleles in population, 2 alleles per genotype
Genotype counts:
AA- 30
Aa- 50
aa- 20
Allele counts
A- 30x2=60 + 50
a- 20x2=40 + 50
what are the four forces of evolution
mutation, natural selection, gene flow, genetic drift
mutation
random changes in the code, only true source of new alleles, can be spontaneous or induced Point mutation, which is when a nitrogen base, adenine (A), thymine (T), cytosine (C), or guanine (G) is replaced. Another type of mutation is a frameshift mutation. This is when rather than the replacement of a nitrogen base, a nitrogen base is inserted or deleted. The third type of mutation is chromosomal. Chromosomal mutation consists of error that occurs during the meiosis of sex cells and you result in more chromosomes. These mutations are very rare so they do not heavily affect allele frequencies.
natural selection
The second force of evolution is natural selection. Natural selection is not random, it is entirely dependent on the environment. It occurs when there are different levels of fitness, or measure of how many offspring an individual has produced. There are three types of selection, stabilizing selection, directional selection, and disrupting selection. Stabilizing selection is when one of two extreme phenotypes is selected for, directional selection is when phenotypes at both extremes are selected against and disruptive selection in the middle range are selected against. Natural selection can cause micro evolution, or change in allele frequency over a long period of time.
gene flow
less random, spread of genetic material between populations, decreases differences in allele frequencies between groups increases diversity within groups, non-random we can predict what will happen
genetic drift
random change in allele frequencies from one generation to the next, based on the law of probability all about chance, increases allele frequency between groups, diversity within a group decreases,
founders effect
when a new population is established by a small number of individuals who are not genetically representative or the large population
reproductive isolation
biological barriers that prevent different species from interbreeding
microevolution
small changes from generation to generation
macroevolution
small changes accumulate to lead to big changes in species
population
a group of individuals living and interbreeding in the same area d
deme
a local population of organisms that have similar genes, interbreed and produce offspring
species
individuals who are capable of breeding with each other and producing viable fertile offspring
translocation
non homologous chromosomes exchanging DNA segments during meiosis
steps in DNA replication
DNA unzips, each strand is a template for assemble of new complementary strand
polygenetic traits
characteristics influenced by two or more genes
tRNA
seeks complementary triplet strands of mRNA codons, contains codons that correspond to specific amino acids, brings amino acids together
dominant allele
masks ressecive trait,
what does DNA replication produce
two identical copies of itself
mendel's law of dominance
one allele masks the effect of another allele