Biological, Prenatal, Birth Flashcards
Where is the chromosome located? Define it.
Chromosomes are located in the nucleus. It stores and transmits genetic information.
What is the difference between phenotypes and genotypes? Define it.
Which depends on which?
Phenotype=observable characteristics
Genotype= genetic information that determines our species and influences unique characteristics.
Phenotypes depend on our Genotypes
How many chromosomes do humans have? Where do they come from?
We have 23 matching pairs (except XY in males). There is 46 in total. One of each is inherited by mother and father.
What are chromosomes made of?
Chromosomes are made of DNA
Approx how many genes lie along a human chromosome?
20-25 thou
We share how much of our DNA with chimpanzees? How about other humans?
98-99%
99.1%
What is a gene?
A gene is segments of DNA along the length of the chromosome.
DNA duplicates itself through which process?
It duplicates itself through Mitosis, which allows diversity though division of cells.
Explain Mitosis. What’s the result of it?
DNA duplicates itself through Mitosis. It permits a single cell, formed at Conception to develop into a complex human which is composed of many cells.
As a result, each new body cell has same number of chromosomes and identical gene info.
Explain DNA. How does our body receive genetic instructions?
this double stranded molecule has a pair of chemical substance called BASE (AT CG). The sequence provides genetic instructions.
According to the book, 99% of heredity is responsible for traits that make us human.
False. According to the book, only a small portion of heredity is responsible for traits that make us human. Like or upright gait language and cognitive capacities.
Concerning base in our DNA, how much change is needed to influence human traits?
One change is a single base pair can influence traits. It can affect multiple genes through Mitosis when it starts to amplify variability in human.
Name all the sex cells w short description.
Autosomes -22 NON sex chromosomes
Sex-XX XY. 23rd pair. Determines sex. X carries most genes. Sex is determined by whether an X or Y bearing sperm fertilizes the ovum.
Gametes- sperm and ova.
Zygote. Sperm and ova united at fertilization.
What is Gametes?
How are gametes formed?
When they are formed, what is it?
New individuals are created when 2 Gametes(sex cells) aka sperm and ova, combine.
Gametes are formed through cell division called Meiosis, which halves the normal # of chromosomes. Sperm and ova which contain 23 each.
When sperm and ovum unite at fertilization, the resulting cell Zygote, will again have 46 chromosomes.
When does crossing over occur? Explain the process. What does this process do.
Crossing over occurs during Meiosis stage. This is when chromosomes which have paired up, and each break a point along their lengths and exchange genes. This exchange allows genes to replace each other in order to combine new hereditary combos.
Explain the 7 step process of Meiosis. Start w original cells and end with zygote period.
1 og cells starts with 4 separate strands of chromosomes. There are 23 pairs each.
2 chromosomes each duplicate and pair with another.
3 crossing over takes place between 2 innermost pair members to exchange genes.
4 the crossovered pairs separate to form 2 cells, each with 23 duplicated chromosomes.
5 duplicated chromosomes separate to form gametes, each with 23 single chromosomes.
6 fertilization
7 zygote. Sperm and ovum unite. First cell of the new individual, the zygote, has 46 or 23 pairs. Same as original cell.
How are monozygotic twins made? How often are they created? How does environment affect it?
When a duplicating zygote separated into 2 clusters of cells, which developed into 2 individuals w the same genetic makeup.
1 in 330 births.
Environment such as temperature oxygen levels and late fertility and genetics.
How are fraternal or dizygotic twins created? What’s their genetic similarities? What are some causes to this? How often?
Release and fertilization if 2 ova. Genetically, they are no more alike than reg. siblings.
Older age fertility drugs and vitro fertilization. 1 in 60.
What is an allele. What are the 2 diff. Descriptions?
What does it determine?
What is a carrier?
Forms of same gene on pair is chromosomes.
Homozygous- 2 alleles the same (each parents alike) and heterozygous- alleles differ.
This determines phenotype.
A carrier is someone with just one recessive allele (Db) that pass their trait.
T or f? Most serious diseases occur due to dominant alleles.
False. It usually occurs with recessive. Our evolution was able to weed it out before reproduction age but some like hunting tons disease remained as dominant bc symptoms don’t occur until 35.
Explain incomplete dominance.
That’s when both genes from parents are inherited and both allele express phenotype.
What is an x linked inheritance?
Males are most likely to receive a recessive gene carrying disorders due to their short Y chromosomes which lacks any corresponding allele to override. Since females have another X chromosomes, they fare better.
T or f? When alleles are imprinted, it is guaranteed to pass on.
Imprinting is temporary.
True
False
T or f. Mutation is a slow process in which our genes create to fight other cells.
Germline mutation is when affected person passes it on.
Somatic mutation is when normal cells mutate at any point in life.
Most defects occur during mitosis.
F. It’s a sudden and permanent change in segment of DNA.
True
True.
False. Most genetic defects occur during Meiosis.
Define polygenic.
Many genes determine characteristics.
How does Down syndrome occur? Does it occur during meiosis or mitosis?
Failure of seperation the 21st pair of chromosomes during meiosis. So the person inherits 3 instead of the 2 normal chromosomes.
Which sex chromosome abnormality produces webbed neck and sterility and spatial intelligence?
Tallness and impaired verbal intel given?
XO
XXX
What is genetic counseling designed for?
Assess chances of having bb w hereditary disorders.
To choose best course of action in terms of risk and family goals.