Science: Genes and DNA

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52 Terms

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adenine (A)

A nitrogen-rich base that forms a pair with thymine (T).

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alleles

Different forms of the same gene located at the same point of homologous chromosomes.

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autosomes

All the chromosomes in a cell other than the sex chromosomes.

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carcinogen

A mutagen that can lead to cancer.

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centromere

The point on a chromosome where the two chromatids are joined together.

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chromatid

One of the strands of a chromosome following replication.

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chromosomes

Thread-like structures in the nucleus composed of DNA and proteins; contains genetic information in the form of genes.

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complementary base pairs

A pair of bases that can join to make the rungs of the DNA ladder—adenine and thymine, guanine and cytosine.

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cytosine (C)

A nitrogen-rich base that forms a pair with guanine (G).

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deoxyribonucleic acid (DNA)

A double helix made of nucleotides; the molecule that determines the genetic characteristics of most living things.

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deoxyribose sugar

One of the parts that make up a nucleotide.

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diploid number

The number of chromosomes in body cells; two sets or 2n.

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DNA profiling

A pattern of DNA fragments unique to each individual.

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dominant trait

The trait that is observed in the outward appearance of a heterozygous individual.

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double helix

Shape like that of a twisted rope ladder.

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gametes

Sperm and egg cells.

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gene

A section of DNA that carries the genetic code for a particular characteristic.

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gene splicing

The process used to add a gene into or remove genes from DNA.

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gene therapy

The process of replacing a defective gene with a normal gene.

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genetically modified

Having the genes changed.

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genetics

The study of inherited characteristics called traits.

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genome

The complete set of DNA including all the genes of a cell, individual, or species.

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genotype

Genetic information carried by an individual.

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guanine (G)

A nitrogen-rich base that forms a pair with cytosine (C).

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haploid number

The number of chromosomes in gametes; one set or n.

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heterozygous

Having two different alleles on homologous chromosomes.

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homologous chromosomes

Chromosomes with genes for particular characteristics at the same location.

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homozygous

Having two identical alleles on homologous chromosomes.

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induced pluripotent stem cells (iPSCs)

Cells that have been made to revert to pluripotent state by the introduction of certain genes.

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meiosis

The type of cell division that produces gametes with half the number of chromosomes of the parent cell.

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mitosis

The type of cell division that produces two daughter cells identical to the parent cell.

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mutagen

An agent that causes a mutation.

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mutation

A mistake that happens as DNA is copied, causing a change to the base sequence.

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nitrogen-rich base

Part of a nucleotide; the four types are adenine (A), guanine (G), cytosine (C), and thymine (T).

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nucleotides

The building blocks of DNA; comprised of deoxyribose sugar, a phosphate group, and a nitrogen-rich base.

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pathogen

A disease-causing organism.

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pedigree

A diagram used to show patterns of inheritance over generations.

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phenotype

Observable characteristics of the individual; the way the genotype is expressed.

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phosphate group

One of the parts that make up a nucleotide.

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plasmid

A ring of DNA found in bacteria.

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pluripotent embryonic stem cells

Stem cells that are capable of becoming any one of the 200 or so different cell types found in the human body.

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pure breeding

Where all individuals have the same genetic information for a characteristic generation after generation.

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recessive trait

The trait that remains hidden in the heterozygous condition and seen only in the homozygous condition.

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recombinant DNA technology

Technology that allows DNA to be recombined with other genes.

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replication

The process of making copies of DNA.

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sex chromosomes

The chromosomes that determine the sex of an individual; in humans they are the X and Y chromosomes.

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sex-linked genes

Genes present on the sex chromosomes.

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single nucleotide polymorphism (SNP)

Locations on chromosomes that differ by only one base from one human to another.

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thymine (T)

A nitrogen-rich base that forms a pair with adenine (A).

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traits

Inherited characteristics.

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Watson–Crick model

The double helix structure of the DNA molecule.

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zygote

The cell formed by fusion of two gametes, a sperm and an egg.