chapter 6-8 Flashcards

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1
Q

what are chromosomes

A

Chromosomes are condensed single molecules of DNA with associated proteins.

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2
Q

what are genes

A

Genes are sequences of bases located on chromosomes that code for specific proteins. These proteins control a particular characteristic or trait of the organism.

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3
Q

what are alleles

A

alleles the different forms of a particular gene

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4
Q

what is a genome

A

A genome is the complete set of genetic instructions for an organism; it is the total DNA of an organism.

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5
Q

Telocentric

A

Centromere is positioned at the tip of the chromosome

No p arms

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6
Q

crossing over

A

involving the exchange of corresponding segments of non-sister chromatids of homologous chromosomes

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7
Q

independent assortment

A

formation of random chromosome combinations during meiosis that contributes towards producing variation

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8
Q

stages of meiosis

A

interphase:
-dna rep
-growth

prophase:
-chromosomes condense
-crossing over
-nuclear envelope degrades

metaphase:
line up along the equator of the cell

anaphase:
they are separated from each other and their centromeres are pulled to opposite poles of the cell by spindle fibres

telophase:
a nuclear envelope reforms around each set of chromosomes (cytokinesis)

anaphase 2:
replicated chromosomes are separated into single stranded ones by the spindle fibres pulling sister chromatids

telophase 2:
forming 4 haploid daughter cells

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9
Q

incomplete dominance

A

“blending” Pink flowers

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10
Q

codominance

A

equal expression AB blood type

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11
Q

epigenetics

A

the study of changes in organisms caused by modifications of gene expression rather than alteration of the genetic code itself
Epigenetic factors can change how DNA in cells is packaged or how it is labelled.

Packaging of DNA in cells may be tight or may be open (see subtopic 6.2). Genes in segments of DNA that are tightly packaged are silenced, while genes in segments of DNA with open packaging are active and translated into protein.

Labelling DNA is like adding a ‘tag’ that does not alter the base sequences of genes, but can either silence genes or make them active.

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12
Q

hemizygous

A

a person who has only one copy of a gene rather than the usual two copies.

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13
Q

monohybrid cross

A

monohybrid cross a cross in which alleles of only one gene are involved

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14
Q

linkage group

A

linkage group genes that are physically close to each other on a chromosome and are likely to be inherited together as a single unit

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15
Q

linked genes

A

Are two gene loci linked?
This can be explored by a particular test cross of a known double heterozygote (AaBb) with a double
homozygous recessive (aabb).
 If the two gene loci are not linked, the genes will assort independently, and the outcome of
the test cross will be four classes of offspring in equal proportions.

 If the two gene loci are linked, the outcome of the test cross can reveal that linkage. There
will be four classes of offspring but the proportions of these will not be equal. Instead, there
will be an excess of offspring from parental gametes and a deficiency of offspring from
recombinant gametes.

Because the loci of two linked genes are physically close, the particular combination of alleles of the
genes that are present on parental chromosomes tend to be inherited together more often than
alternative combinations. These combinations of alleles can, however, be broken by crossing over
during meiosis so that new combinations of alleles are generated. The chance that this occurs
depends on the distance between the two linked genes.

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16
Q

Chiasma

A

Chiasma is the point of contact between two non-sister chromosomes belonging to the homologous chromosomes.

17
Q

haploid and diploid cells

A

Haploid refers to the presence of a single set of chromosomes in an organism’s cells. Sexually reproducing organisms are diploid (having two sets of chromosomes, one from each parent).

18
Q

test cross

A

test cross a cross used to determine the genotype of an individual with an unknown genotype by crossing it to an individual with a homozygous recessive genotype

19
Q

dihybrid

A

A dihybrid cross involves the alleles of two different genes

20
Q

zygote

A

zygote, fertilized egg cell that results from the union of a female gamete (egg, or ovum) with a male gamete (sperm).

a cell formed by the union of two gametes

21
Q

Nucleotide

A

Nucleotides refer to the foundation of nucleic acids such as the polymers DNA and RNA. It is basically composed of a sugar molecule connected to a phosphate group of the nitrogen-containing bases.

22
Q

Polypeptide

A

They are the building blocks of proteins

23
Q

Non-disjunction

A

a pair of homologous chromosomes has failed to separate or segregate at anaphase so that both chromosomes of the pair pass to the same daughter cell.