Reproduction, DNA, Genetics, and Mutations Flashcards

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Flashcards covering key vocabulary related to sexual and asexual reproduction, human reproductive systems, DNA, genetics, and mutations.

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64 Terms

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Sexual Reproduction

Involves the union of sex cells (gametes) to form a zygote (a single fertilised cell).

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Gametes

A sex cell (sperm or ovum) which is a haploid reproductive cell of an organism.

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Zygote

The diploid, single cell that is formed at fertilisation.

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Gonads

An organ (testis or ovary) which produces sex cells.

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Asexual Reproduction

The production of offspring without involving sex cells (gametes).

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Menstrual Cycle

A recurring cycle of hormonal changes in females, averaging 28 days, involving menstruation and ovulation.

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Menarche

The first menstrual cycle in females.

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Menopause

The cessation of menstruation in females.

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Ovulation

The process of the ovum being released from a follicle in the ovary in the middle of the menstrual cycle.

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FSH (Follicle Stimulating Hormone)

A hormone produced by the pituitary gland that promotes follicle development and ovum maturation.

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LH (Luteinising Hormone)

A hormone from the pituitary gland that triggers ovulation.

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Oestrogen

A hormone produced by ovarian follicles that thickens the uterine lining.

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Progesterone

A hormone secreted by the corpus luteum that maintains the uterine lining.

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Foetus

An embryo after 8 weeks of development.

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DNA (Deoxyribonucleic Acid)

A complex molecule containing the genetic blueprint for an organism.

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Nucleotide

The basic building block of DNA, consisting of a sugar, a phosphate group, and a nitrogenous base.

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Nitrogenous Bases

Adenine (A), Thymine (T), Guanine (G), and Cytosine (C), which form the genetic code in DNA.

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RNA (Ribonucleic Acid)

A nucleic acid that plays various roles in genetic processes, including protein synthesis.

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Chromosomes

Tightly coiled DNA structures found in the nucleus of cells.

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Autosomes

Non-sex chromosomes.

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Sex Chromosomes

Chromosomes that determine biological sex (XX for females, XY for males).

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Centromere

The region of a chromosome where sister chromatids are joined.

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Genes

DNA sequences on chromosomes that code for proteins.

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Alleles

Alternative versions of a gene.

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Karyogram (Karyotype)

An image of chromosomes arranged in homologous pairs based on size, centromere position, and banding patterns.

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DNA Replication

The process of duplicating DNA before cell division.

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Somatic Cells

Body cells that contain chromosomes in pairs (diploid).

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Diploid (2n)

Having two sets of chromosomes.

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Haploid (n)

Having one set of chromosomes.

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Mitosis

Nuclear division that produces diploid body cells for growth, repair, and replacement.

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Meiosis

Nuclear division that produces haploid sex cells in the gonads for reproduction.

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Cytokinesis

The division of the cytoplasm and whole cell into two new diploid daughter cells.

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Inheritance

The passing of traits from one generation to the next.

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Genetics

The study of inheritance.

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Complete Dominance

A type of inheritance where a dominant allele completely masks a recessive allele.

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Genotype

The symbolic representation of the alleles possessed for a particular trait.

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Homozygous

Both copies of an allele are the same.

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Heterozygous

Both copies of an allele are different.

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Phenotype

The visible affect of the genotype possessed.

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Pedigrees

Illustrations of inheritance patterns within families to determine if a trait is dominant or recessive.

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Autosomal Inheritance

Inheritance of traits located on autosomes (non-sex chromosomes).

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Sex-Linked Inheritance

Inheritance of traits via sex chromosomes (X or Y).

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Punnett Square

A grid used to predict genotypes and phenotypes in genetic crosses.

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Incomplete Dominance

A heterozygous individual shows a blended phenotype.

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Codominance

Both alleles are fully expressed in a heterozygous individual.

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Protein Synthesis

The process of constructing proteins based on genetic instructions carried by DNA and RNA.

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Central Dogma of Biology

DNA → RNA → Protein.

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mRNA (Messenger RNA)

Transcribes genetic code from DNA and carries it to ribosomes.

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rRNA (Ribosomal RNA)

Forms the core of ribosome's structure and facilitates protein synthesis.

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tRNA (Transfer RNA)

Brings amino acids to ribosomes during translation to form proteins.

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Transcription

The process of copying DNA into mRNA.

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Translation

The process of decoding mRNA to synthesize proteins.

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Mutations

A change to the DNA sequence in genes and chromosomes.

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Mutagens

Environmental agents that cause mutations.

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Gene Mutations (Point Mutations)

Small-scale changes in the DNA base sequences within genes.

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Chromosome Mutations

Larger-scale mutations that include whole extra or missing chromosomes or significant deletions or translocations of chromosome sections.

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Substitution

A gene mutation where one base is replaced by another.

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Inversion

A gene mutation where a sequence of bases is flipped.

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Insertion

A gene mutation where additional bases are added, causing a frameshift.

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Deletion

A gene mutation where bases are removed, causing a frameshift.

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Aneuploidy

An abnormal number of chromosomes in a cell.

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Monosomy

The presence of only one copy of a chromosome instead of the usual two.

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Trisomy

The presence of an extra chromosome, leading to three copies.

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Non-disjunction

The failure of chromosome pairs to separate properly during cell division.