science Flashcards

(51 cards)

1
Q

Gregor Mendel

A

discovered the basics of genetics.
1842 – Enters monastery
Background of mathematics and science
Had a small garden
Studied Pea plants

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2
Q

Mendel’s Methods: how many characteristics did he study?

A

Seven characteristics each with two contrasting traits.

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3
Q

Pollination

A

pollen grain goes from the male anther and lands onto female stigma

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4
Q

Anthers

A

This is the top part of the male strcture (part that produces pollen grains, their also sperm?

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5
Q

Stigma

A

top of the female structure.

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6
Q

Cross-pollination

A

pollen goes from the flower of one plant and lands on the flower of another plant.

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7
Q

self pollination

A

Since they are perfect flowers, they have both the male and female strucures, so they are able to self pollinate.

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8
Q

Perfect flower:

A

Type of flower that has both the male and female structure in the flower. Perfect flowers are capable of self pollination, which also means their offspring are genetically identical

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9
Q

What is the product of cross pollination

A

hybrids.

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10
Q

Allele

A

possibility of trait. Each parent donates one allele to their offspring.

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11
Q

Principal of dominance

A

YOUR PHENOTYPE (physical appearance) IS DETERMINDED BY YOUR GENOTYPE.

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12
Q

Law of Segregation

A

the two alleles will seperate during the formation of the gammetes.

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13
Q

Law of Independent Assortment

A

“The inheritance of one trait does not influence the inheritance of another trait” Mendel

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14
Q

mendalian

A

A trait is controlled by a single gene, that gene has two possible alleles, with 3 possible genotypes, with 2 possible phenotypes.

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15
Q

What three laws did Mendel create/prove:

A

Principle of Dominance,
Law of Segregation
Law of Independent Assortment

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16
Q

Dihybrid

A

An organism that is heterozygous for both of two traits, with another organism that is heterozygous for both of two traits. (EX: BbCc, with BbCc) mating two individuals who are identically heterozygous for two distinct traits

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17
Q

Monohybrid=

A

a genetic mating between two organisms that investigates the inheritance pattern of a single, specific trait

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18
Q

Genetic Disorders Caused by Single Allele: Dominant

A

Huntington’s disease

Polydactyly

Marfan’s Syndrome

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19
Q

Genetic Disorders Caused by Single Allele: Recesive

A

Albinism

Cystic fibrosis

Phenylketonuria

Tay-Sachs

Sickle Cell Disease

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20
Q

SIMILARTYS BETWEEN, MENDELLEAN, CODOMINANCE, AND INCOMPLETE DOMINANCE:

A

ONLY ONE GENE CONTROLS ALL TRAITS
ONLY TWO POSSIBLE ALLENES PER TRAIT.
3 POSSIBLE GENOTYPES

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21
Q

DIFFERENCES BETWEEN MENDELEAN CODOMINCANCE AND INCOMPLETE:

A

2 PHENOTYPES FOR MENDELEAN, 3 PHENOTYPES FOR INCOMPLETE AND CODOMINANCE.

22
Q

genotype

23
Q

phenotype

24
Q

codominance

A

When heterozygous offspring contain both traits that are dominant so they both show, (this time seperate, ex: red flower+ white flower= flower with both red and white pedals)

25
incomplete dominance
When heterozygous offspring contain a mix of two traits together (white flower+ red flower=pink flower)
26
multiple alleles
more than two possible alleles. Still comes from one gene. Number of phenotypes equal to number of alleles
27
polygenic inheritance
means multiple genes
28
who studied fruit flies
Thomas hunt Morgan
29
Thomas hunt Morgan
Discovered some traits are inherited together (ex: normal color of eyes is red. There is a simple non-lethal mutation where their eyes are white. HE ALSO SAW IT WAS MOSTLY MALES WITH WHITE EYES.)(this means the eye color gene was on the sex chromosome) Genes on the same chromosome are linked= gene linkage. They are inherited together
30
How does our understanding of meiosis challenge mendel?
previous statement of independent assortment was disproven. Its sot genes that are assorting independently but chromosomes, and if genes are on the same chromosome their often inherited together?
31
updated def for independent assortment
When traits are on separate chromosomes they will be inherited separately, when trait are on the same chromosome they are linkeda and often inherited together, unless they cross over in prophase one.
32
why did mendel get it wrong?
Mendel got it wrong since he had no acknowledgement of chromosomes, and the seven traits he studied were all on different chromosomes.
33
How can genes on the same chromosome be inherited separately?
When crossing over takes place in prophase one!
34
Male vs Female sex traits. what does the Y chromsome do.
Y TRAIT IS ONLY SEX DETERMINATION
35
Hemophelia
cannot make factor 8, dont have that clotting factor. Different from sex influenced traits
36
Muscular dystrophy
sex linked recessive allele with protein not being produced. Color-blindness
37
autosomal trait
38
Karyotype
: shows the gender and the amount of chromosomes
39
NONDISJUNCTION
failure of chromosomes to separate
40
nonjunction mieosis 1 vs 2
If nonjunction happens in meiosis one than theres two gametes with 3 chromosomes, and 2 with 1 If nonjunction happens in meiosis two than their is one gamete with 3, one with 1, and 2 with two
41
Trisomy
means three chromosomes where their should be two
42
Monosomy
1 chromosome where their should be two
43
Polyploidy
more than two sets of chromosomes.
44
only monosmy that can live
Turner syndrome: They have only ONE sex chromosome (X). They are female, with little differences only maybe in puberty. Most gerastic symtom is that they are sterile,
45
KLINEFELTER’s SYNDROME
a case of trisomy involving the sex chromosomes. (XXY) often looks very typical but is also sterile and can’t have children.
46
Barr bodies
Inactive X chromosome.(Happens when there is more than one X chromosome. predominantly occurs in females, what happens is only ONE X is activated,
47
Chromosomal mutations
Insertion, Deletion, Inversion, Translocation
48
insertion and deletion definitions:
Insertion: a duplicated gene on its homologous chromosome. (ex: one has no A gene, other chromosome has two A gene) Deletion: because of improper crossing over, a gene is lost(deleted) usually a duplicate on its homologous chromosome.
49
Inversion, Translocation defintions
Inversion: if crossing over takes place they could be reinserted in the reverse orientation. (ex: normal=a,b,c,d. inversion=a,b,d,c) Translocation: when there is crossing over between non-homologous chromosomes.
50
what do all chromosomal mutations have in common? (insertion, deletion, inversion, translocation)
almost always made by a mistake in crossing over Impacts genes on the chromosome and impacts will vary
51
IMPORTANT TO REMEMBER> this is the fuh ass body paragraph about how the discovery of genetics changed over time
Starts with mendels work with pea plants where he discoveres the 3 laws, (define them) in the end finding out about autosomal genetics. Next we found out about incomplete dominance and codomianc (define them) which disproved the previous mendelian statement (each trait is defined by one gene which has 3 possible genotypes, and 2 mossible genotypes.) next there was the discovery of multiple alleles (give example and def) along with polygenic traits (define and example) we changed mendles law of independent assortment when we found chainlinked inheritance, and then sex linked inheritance which proved that some traits have a higher chance of being inheritated together, (more chromosomal) environment can play role, along with nutrition and behavior. Nondisjuntion can also play a role within chromosome and barr bodies, and mistakes with crossing over.