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chromosones
made up of DNA
Autosomes
Any chromosome that is not a sex chromosome
Chromatin
Clusters of DNA, RNA, and proteins in the nucleus of a cell
sex chromosomes
Chromosomes that determine the sex of an individual
Karyotypes
A picture of all the chromosomes in a cell arranged in pairs
Mitosis
part of eukaryotic cell division during which the cell nucleus divides
sister chromatids
joined copies of the original chromosome
centromere
Area where the chromatids of a chromosome are attached
2 parts of cell cycle
interphase and mitosis (cell division)
interphase 3 stages
G1, S, G2
what does g1 phase do
Cell growth
S stage of interphase
DNA replication
G2 stage of interphase
Occurs after DNA has been copied; all cell structures needed for division are made (e.g. centrioles); both organelles & proteins are synthesized
G0 stage of interphase
-Cells become nondividing remain viable and metabolically active but are not proliferative
-can be stimulated to return to G1
duplication division
mitosis, another name
Cytokinesis
division of the cytoplasm
apoptosis
programmed cell death
interphase checkpoints
The checkpoints occur at the end of G1, G2, & M
This happens to make sure that the cell is the right size and that the cell has duplicated the DNA fully
What is the G1 checkpoint
integrity of DNA is checked
what is the G2 checkpoint
no DNA damage, chromosome set complete, enough cell components
what is the mitotic checkpoint
a control point in the cell cycle where "STOP" signals are overridden by "GO" signals
External control
stimulate a cell to divide
parent cell
original cell before cell division
daughter cell
the two new cells that result from mitosis and cytokinesis
centromere
Region of a chromosome where the two sister chromatids attach
Diploid (2n)
two copies of each chromosome
mitotic spindle
An assemblage of microtubules and associated proteins that is involved in the movements of chromosomes during mitosis.
Aster
an array of microtubules
Mitosis phases
prophase, metaphase, anaphase, telophase
prophase purpose
centrosomes duplicate and chromosomes condense, nuclear envelope fragments, and nucleolus disappears.
Prometaphase purpose
spindles attach to centromeres, and chromosomes are placed in the nucleus
Metaphase
The chromosomes line up at the metaphase plate.
Anaphase purpose
centromeres divide, and sister chromatids are now called chromosomes.
Telophase purpose
chromosomes arrive t poles and become chromatin, spindle disappears, nuclear envelope and nucleolus reappears, 2 daughter nuclei.
nucleolus
Makes ribosomes
Cleavage furrow
The first sign of cleavage in an animal cell; a shallow groove in the cell surface near the old metaphase plate.
actin filaments
protein fibers that play a role in cell division and shape
Meiosis
reduction division process, occurring only in reproductive cells, in which one diploid (2n) cell produces four haploid (n) cells that are not genetically identical
homologous chromosomes
Chromosomes that have the same sequence of genes and the same structure
interkenesis
Period of time between meiosis I and meiosis II during which no DNA replication takes place.
Prophase I
synapsis and crossing over
Spermatogenesis
Formation of sperm
Oogenesis
The production of mature egg cells.
How many sperm are made per min?
300,000 sperm
How many sperm are made per day?
400 million
spermatids
four haploid cells that are formed when a diploid reproductive cell divides meiotically
Spermatozoa
a mature sperm cell
Polar body
holds discarded chromosomes.
Allele
Different forms of a gene
Nondisjunction
Error in meiosis in which homologous chromosomes fail to separate.
Trisomy
extra chromosome 2n + 1
Monosomy
missing a chromosome (2n-1)
Trisomy 21
Down syndrome
Are trisomy usually fatal
yes
Barr body
Inactivated X chromosome
Turner Syndrome
A chromosomal disorder in females in which either an X chromosome is missing, making the person XO instead of XX, or part of one X chromosome is deleted.
Jacob's Syndrome
XYY males, nondisjunction during meiosis II
who is likely to have a child with trisomy 21
women over 40.
down syndrome symptoms
- Intellectual Disability (#1 Cause)
- Epicanthal Folds (Eyes)
- Flat Facies
- Single Palmar Crease
- Gap Between 1st-2nd Toe
- Duodenal Atresia
- Hirschsprung Disease
- Heart Disease (Septal Defects)
syndrome
A group of symptoms typical of a particular disease or condition
SRY gene
sex determining region of the Y chromosome
Testis Determining Factor (TDF)
protein encoded by a gene in the SRY that triggers testes formation
Klinefelter syndrome
47, XXY
female poly x syndrome
more than 2 x chromosomes and extra Barr bodies
Deletion
part of a chromosome is missing
inversion
segment of a chromosome is inverted
duplication
the presence of a chromosomal segment more than once in the same chromosome
Translocation
movement of a segment from one chromosome to another nonhomologous chromosome
nonhomologous
nonmatching chromosomes
Williams syndrome
chromosome 7 loses a tiny end piece
Cri du chat syndrome
deletion on chromosome 5
tetralogy of fallot
congenital malformation involving four distinct heart defects
Clubbing
widening of the fingertips