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Mitosis
the process of cell division that results in two identical daughter cells from a single parent cell in somatic cells
Interphase, prophase, metaphase, anaphase, and telophase
Stages of mitosis in order
Interphase
initial stage of the cell cycle; cell spends the most amount of time here
Prophase
longest phase of mitosis; centrioles migrate to opposite ends of the cell to establish poles
Metaphase
chromosomes line up at the middle of the cell; produces spindle fibers
Anaphase
spindle fibers pull chromosomes apart at the centromeres; half sister chromatids moves in opposite direction
Telophase
final stage; cytokinesis divides the cytoplasm of the cells into two
Chromatin during ______ is replicated; unwound chromosome located in nucleus
Interphase
Sister chromatids held together at the centromere during _______
prophase
____ new identical daughter cells are formed containing 2N number of chromosomes during _______
Two, Telophase
Meiosis
occurs in gametes or sex cells to produce daughter cells with half the number of chromosomes as usual
______ has two cell divisions, resulting in 4 genetically unique daughter cells
Meiosis
Interphase, Prophase 1, Metaphase 1, Anaphase 1, Telophase 1, Prophase 2, Metaphase 2, Telophase 2
Stages of meiosis in order
Crossing Over
During prophase 1 replicated homologous pairs of chromosomes come together in a process called synapsis, where sections of chromosomes are exchanged
Where does mitosis occur
In body cells
Where does meiosis occur
in testes and ovaries (sex cells)
What is the final product in mitosis
2 diploid cells
What is the final product in meiosis
Four gametes haploid cells
IF AN ORGANISM HAS A DIPLOID NUMBER OF 16, HOW MANY CHROMATIDS ARE VISIBLE AT THE END OF MITOTIC PROPHASE?
32
Metacentric
The centromere is located approximately in the middle, dividing the chromosome into two equal arms.
Acrocentric
The centromere is positioned very close to one end, resulting in a very short p-arm.
Telocentric
The centromere is located at the very tip or end of the chromosome
True Breeding
parents whose offspring are identical for a certain trait
Reciprocal cross breeding
designed to test the role of sex on the inheritance pattern
Postulate 1
a specific unit factor exists for each trait, receiving one factor from dad and one from mom
Postulate 2
when two different unit factors are present for an individual, one factor is dominant to the other
Postulate 3
during meiosis, the paired unit factors separate/segregate randomly
Gene
the modern term for mendel's “unit factors” unit of inheritance
Allele
Alternative form of a gene
Test Crossing
taking an individual with an unknown genotype and crossing it with a known genotype (homozygous recessive)
Postulate 4
pairs of contrasting traits are inherited independently
Homogametic
sex-produce uniform gametes (ex. Females in mammals)
Heterogametic
sex-produce unlike gametes (ex. Males in mammals)
Monohybrid Cross
¾ dominant ¼ recessive
When answering a chi-square what must you include
Full chi-square table, degrees of freedom, null hypothesis, conclusion fail to reject or reject
Incomplete or Partial Dominance
when a cross between two parents with different phenotypes produces an intermediate phenotype; neither parental allele is dominant
Codominance is only in a ________
heterozygote
Hemizygous
males cannot be homozygous or heterozygous for x-linked genes because they only have one copy of the x chromosomes
Sex chromosomes in birds
Female-ZW Male-ZZ
Sex Linked traits
Traits that are located on the sex chromosomes only, x linked in humans/mammals and z linked in birds, males in humans/mammals and females in birds only have one allele for each gene, not two
Sex Limited inheritance
Occurs on autosomal chromosomes, NOT the sex chromosomes, Expression of a specific phenotype is absolutely limited to one sex, Expression of the gene is turned off in one of the sexes despite having the same genotype, Responsible for sexual dimorphism-observable differences between sexes
Sex Influenced Inheritance
Occurs on autosomal chromosomes, NOT the sex chromosomes, The sex of the individual influences the expression of a phenotype that is not limited to one sex or the other, The expression of the gene in sex influenced traits is influenced by a hormonal or anatomical difference between sexes, Heterozygous genotype exhibits one phenotype in one sex and contrasting one in the other , An allele may be expressed as a dominant in one sex and recessive in the other
Primary First Division Nondisjunction
failure of paired homologous chromosomes (tetrad) to separate during the first meiotic division
Secondary Second Division Nondisjunction
failure of sister chromatids to divide during the second meiotic division
What is the result of First Nondisjunction
Results in both trisomy and monosomy
What is the result of Second Nondisjunction
Results in all 3 conditions-trisomy,disomy, and monosomy
Result of Nondisjunction
Egg or sperm cell can lose a sex chromosome resulting in a daughter with only one X chromosome
Aneuploidy
the abnormal condition where one or more chromosomes of a normal set of chromosomes are missing or present in more than their usual number of copies

Monosomy X-Turner Syndrome
1st Type of chromosomal # abnormality, characterized by short stature, unable to conceive, kidney problems

Trisomy 21 Downsyndrome
2nd type of chromosomal # abnormality
Disomy
No loss or gain of chromosomes have occurred-normal meiotic division
Lethal Alleles
Genes which result in viability reduction of an individual or become a
cause of death to individuals carrying them