Unit 5 Flashcards

1
Q

Haploid

A

A cell that only contains 1 chromosome. (n)

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2
Q

Gamete

A

A sex cell (haploid). Examples include sperm and egg.

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3
Q

Dipold

A

A cell that has 2 sets of chromosomes. (2n)

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4
Q

Homoglous chromosomes

A

a pair of chromosomes in a diploid organism that have the same genes in the same order, meaning they are similar in structure and size, with one chromosome coming from the mother and the other from the father.

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5
Q

Gregor Mendel and Mendelian genetics

A

Gregor Mendel discovered genetics. And Medelian genetics A type of genetic allelle meant the dominant allele was expressed.

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6
Q

Homozygous

A

They share 2 same alleles.

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7
Q

Heterozygous

A

Different versions of homoglous chromosomes.

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8
Q

Phenotype

A

The expressed physical traits.

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9
Q

Genotype

A

The genetic combination. (Combo of alleles)

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10
Q

Dominant Alleles

A

Alleles can be dominant or recessive. You can only see the phenotype of the dominant.

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11
Q

P Generation

A

Paternal generation.

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12
Q

F1 generation

A

All hybrids; all heterozygous. Offspring of P generation.

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13
Q

F2 generation

A

Grandchildren of P generation, children of F1 generation. Offspring of a cross between hybrids.

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14
Q

Law of segregation

A

Allells separate independently during meiosis which allows for a different combination of alleles.

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15
Q

Law of independent assortment

A

During gamete formation different pairs of alleles segregate independently of eachother. The given allele from your mother or father is completely random and is not effected by the alleles of the other parents.

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16
Q

Monohybrid cross

A

A genetic cross eximinaing a single trait.

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17
Q

Dihybrid cross

A

A genetic cross examining 2 traits.

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18
Q

Linked Genes

A

Genes located close together on the same chromosome tend to be inherited together because they are less likely to be
separated during crossing over in meiosis. This reduces the independent assortment of these genes. It is impossible for linked genes to be on different chromosomes.

19
Q

Barr Bodies

A

Barr bodies help determine X chromosome
abnormalities in conditions like Turner syndrome (XO) or
Klinefelter syndrome (XXY)

20
Q

Co-dominace

A

When both alleles are expressed at the same time, but do no blend! So there may be white portions of a flower and red portions of a flower.

21
Q

Complete Dominace

A

Dominance where the homozygous completely masks the heterozygous and phenotypically look the same.

22
Q

Sex-Linked genes

A

Traits and diseases that are more likely to occur in one sex over the other. Mostly sex-linked traits are found on the X chromosome. Which is especialy detrimental to males as they only have one X. Females can be carriers.

23
Q

Allele

A

A version of a gene. (i.e purple or white flowers different versions of the color gene.)

24
Q

Non-Mendelian genetics

A

A type of genetic inheritance that is more nuanced compared to Mendelian. It includes Co-dominant.

25
Q

Somatic cell

A

Any cells other than a reproductive cells.

26
Q

Asexual reproduction

A

Asexual reproduction produces clones that are genetically identitcal to the parent. Low genetic variation but efficient. Somatic cell divison to create a new indepdent somatic cell.

27
Q

Zygote

A

The result of a fusion of a sperm and egg; a fertilized ovum.

28
Q

Fertilization

A

When 2 gametes (haploid) combine to form a zygote (diploid cell).

29
Q

Meiosis I

A

Duplicated parts of homoglous chromosomes are separated. Reducing the chromosome number. Meiosis I begins with one diploid parent cell and ends with two haploid daughter cells.

30
Q

Meiosis II

A

Starts with 2 haploid parent cells then the duplicated chromosomes are then separated. In the end 4 genetically different gametes are produced.

31
Q

Chiasmata

A

The point of contact, the physical link, between two (non-sister) chromatids belonging to homologous chromosomes. Later crossing over occurs.

32
Q

Nondisjunction

A

When chromosomes don’t separate correctly in meiosis/mitosis. The result is a extra or missing chromosome.

33
Q

Autosomal chrosomsomes

A

Chromosomes 1-22 that are not sex chromosomes.

34
Q

Centromere

A

A structure that hold 2 chromatids together. (X)

35
Q

Sex chromosomes

A

X and Y! Non autosomal.

36
Q

Sister Chromatid

A

A sister chromatid refers to the identical copies formed by the DNA replication of a chromosome, with both copies joined together by a common centromere.

37
Q

Iocus

A

Specific location of a gene on a chromosome.

38
Q

Chromatin

A

Chromatin refers to a mixture of DNA and proteins that form the chromosomes found in the cells of humans and other higher organisms.

39
Q

polygenic genes

A

When 2 or more genes determine a trait.

40
Q

Pedigrees

41
Q

tetrad

42
Q

recombination

A

Happens during Meiosis I. The order of genes on a chromosome can be determined using recombination frequencies. Pairs of genes with larger recombination frequencies are typically farther apart, while pairs of genes with smaller recombination frequencies are typically closer together.

43
Q

chiasmata

44
Q

Incomplete dominance

A

Red + White = pink flower, both traits are expressed at the same time and blend.