Essential Genetics Terminology & Concepts

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Essential Genetics Terminology

Conjugation: Genetic Material Transfer

Conjugation is the transfer of genetic material between unicellular individuals through direct cell-to-cell contact.

Bacterial Conjugation: Not Sexual Reproduction

Bacterial conjugation is often incorrectly regarded as the bacterial equivalent of sexual reproduction or mating.

Spermatogenesis: Male Sperm Development

Spermatogenesis is the process by which male spermatogonia develop into sperm cells.

Oogenesis: Female Egg Development

Oogenesis is the process by which female oogonia develop into egg cells.

Monohybrid Cross: Single Trait Inheritance

A monohybrid cross is a method of tracking the inheritance of a single trait from a pair of homozygous grandparents through generation F1 to generation F2.

Mutation: DNA Sequence Change & New Traits

A mutation is a change in the base-pair sequence within the DNA of a gene or chromosome of an organism, resulting in the creation of a new character or trait not found in the wild type.

Autosomal Inheritance: Genetic Transmission Patterns

Autosomal inheritance describes the patterns of genetic transmission related to autosomal genes.

Genetic Ratios: Genotype & Phenotype

  • Genotype Ratios: (2:1:1)n
  • Phenotype Ratios: (3:1)n

Complete Dominance: Both Alleles Dominant

Complete dominance occurs when both alleles are dominant.

Incomplete Dominance: Partial Expression

Incomplete dominance occurs when one allele is dominant and the other is recessive.

Codominance: Heterozygote Exhibits Both Phenotypes

Codominance is when the heterozygote exhibits the phenotypes of both homozygotes.

Overdominance: Heterozygote Fitness Advantage

Overdominance occurs when the dominant relationship is modified, leading heterozygote individuals to develop higher phenotypic fitness than dominant homozygotes.

Multiple Alleles: More Than Two Gene Variants

Multiple alleles exist when there are more than two different alleles of one gene that affect a trait and occupy a given locus.

Pleiotropy: Single Gene, Diverse Effects

Pleiotropy is when a single gene or gene pair produces diverse phenotypic effects.

Gene Penetrance: Dominant Gene Manifestation

Gene penetrance is the frequency with which a dominant gene manifests itself in individuals within a population.

Gene Expressivity: Phenotypic Expression Degree

Gene expressivity is the degree to which a penetrant gene or genotype is phenotypically expressed in an individual.

Lethal Genes: Mutant Alleles Causing Death

Lethal genes are mutant alleles that can cause death.

Complementary Genes: Interacting Gene Pairs

Complementary genes are two interacting non-allelic gene pairs that modify each other's action.

Epistatic Genes: Masking Phenotypic Expression

Epistatic genes represent a form of gene interaction in which alleles of one gene pair mask or inhibit the phenotypic expression of another allele pair.

Polygenes: Multiple Genes, Small Phenotypic Effects

Polygenes are a group of allelic pairs that may affect the same trait, with each producing a small effect on the overall phenotype.

Linkage Group: Genes on the Same Chromosome

A linkage group refers to genes that occur on the same chromosome.

Complete Linkage: Genes Inherited Together

Complete linkage occurs when genes on the same chromosome do not separate and are jointly inherited in gametes.

Incomplete Linkage: Genes Separate in Gametes

Incomplete linkage occurs when linked genes separate and are inherited in different gametes.

Chiasmata: Chromosome Attachment Points

Chiasmata are the points of attachment within a chromosome.

Genetic & Linkage Maps: Gene Positions

A genetic map or linkage map illustrates the relative positions of genes on a chromosome.

Map Units (mu) & Centimorgans (cM)

Map units (mu) define the interval in which one percent of crossing-over takes place; also known as a Centimorgan (cM).

Interference: Chiasma Formation Reduction

Interference describes how one formed chiasma reduces the probability of another chiasma forming in the next chromosomal locus.

Coefficient of Coincidence: Interference Variation

The coefficient of coincidence measures the extent to which interference varies across different segments of a chromosome.

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