Nuclear matters Flashcards

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1
Q

What role does DNA play in inheritance?

A

You get 23 chromosomes from your dad and another 23 from your mother. These chromosomes hold the DNA which in turn makes you who you are, inheriting these from your mum and dad in turn gives you traits they have or traits that laid dormant in their genes.

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2
Q

What is the relationship between DNA, genes, and chromosomes?

A

DNA is deribonucleic acid, it makes up genes and these genes are what determine your traits and these genes are tightly but neatly packed into chromosomes which you have 23 of in every cell of your entire body.

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3
Q

What are karyotypes?

A

A karyotype is a full set of DNA, in a sort of graph that shows every chromosome you have. This can be used to determine certain genetic disorders.

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4
Q

What are Gametes?

A

These are sex chromosomes, males have sperm, females have ova each contains 23 chromosomes. They are produced via meiosis. A XX gives a female a XY gives a male.

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5
Q

Cell

A

The basic structural and functional unit of all living organisms. Cells are the smallest units of life that can replicate independently.

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6
Q

Nucleus

A

A membrane-bound organelle found in eukaryotic cells that contains the genetic material (DNA) and controls the cell’s growth, metabolism, and reproduction.

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7
Q

Chromosome

A

A thread-like structure composed of DNA and proteins that carries genetic information. In humans, chromosomes are found in the nucleus of each cell.

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8
Q

Gene

A

A segment of DNA that contains the instructions for building a specific protein or set of proteins, which in turn determines a particular trait.

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9
Q

Deoxyribonucleic Acid (DNA)

A

The molecule that carries the genetic instructions used in the growth, development, functioning, and reproduction of all known living organisms and many viruses.

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10
Q

Meiosis

A

A type of cell division that reduces the number of chromosomes by half, resulting in four genetically distinct daughter cells. This process is essential for the production of gametes (sperm and ova).

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11
Q

Ova

A

The female gametes or eggs, which are produced in the ovaries and are involved in reproduction.

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12
Q

Sperm

A

The male gametes, produced in the testes, that fertilize the female ova during reproduction.

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13
Q

Mitosis

A

A type of cell division where a single cell divides to produce two genetically identical daughter cells, each with the same number of chromosomes as the parent cell. This process is used for growth and repair.

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14
Q

Fertilisation

A

The process where a sperm cell fuses with an ovum, resulting in the formation of a zygote, which eventually develops into a new organism.

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15
Q

Zygote

A

The initial cell formed when a sperm cell fertilizes an ovum. This cell undergoes multiple divisions and differentiations to develop into a new organism.

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16
Q

Somatic Cells

A

Any cells in the body that are not gametes. These cells make up the organs, tissues, and other parts of an organism’s body.

17
Q

Genotype

A

The genetic makeup of an individual organism, consisting of all the genes and their variants.

18
Q

Phenotype

A

The observable physical or biochemical characteristics of an organism, as determined by both its genotype and environmental influences.

19
Q

Autosomes

A

Chromosomes that are not sex chromosomes. Humans have 22 pairs of autosomes.

20
Q

Sex Chromosomes

A

Chromosomes that determine the sex of an individual. In humans, these are the X and Y chromosomes.

21
Q

X Chromosome

A

One of the two sex chromosomes in humans. Females have two X chromosomes, while males have one X and one Y chromosome.

22
Q

Y Chromosome

A

The sex chromosome found only in males, which, along with the X chromosome, determines male sex characteristics.

23
Q

Homologous

A

Chromosomes that have the same genes at the same loci, but possibly different alleles. One chromosome of each homologous pair is inherited from each parent.

24
Q

Non-homologous

A

Chromosomes that do not pair during meiosis and do not have the same gene sequences.

25
Q

Trisomy

A

A genetic condition where an individual has three copies of a chromosome instead of the usual two. An example is Down syndrome, which is trisomy 21.

26
Q

Monosomy

A

A genetic condition where an individual has only one copy of a chromosome instead of the usual two.

27
Q

Karyotype

A

The complete set of chromosomes in a cell, displayed in a systematic way for analysis. It can be used to diagnose chromosomal abnormalities.

28
Q

Telomere

A

The protective cap at the end of a chromosome that prevents the chromosome from deteriorating or fusing with neighboring chromosomes.

29
Q

Centromere

A

The region of a chromosome where the two sister chromatids are joined together and where the spindle fibers attach during cell division.