The units that determine the inheritance of biological characteristics are

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  • Learning Objectives
    • Describe the structure of a gene and how offspring inherit genes from each parent

    Pairs of Unit Factors, or Genes

    Mendel proposed that paired unit factors of heredity were transmitted faithfully from generation to generation by the dissociation and reassociation of paired factors during gametogenesis and fertilization, respectively. After he crossed peas with contrasting traits and found that the recessive trait resurfaced in the F2 generation, Mendel deduced that hereditary factors must be inherited as discrete units. This finding contradicted the belief at that time that parental traits were blended in the offspring.

    A gene is made up of short sections of DNA that are contained on a chromosome within the nucleus of a cell. Genes control the development and function of all organs and all working systems in the body. A gene has a certain influence on how the cell works; the same gene in many different cells determines a certain physical or biochemical feature of the whole body (e.g., eye color or reproductive functions). All human cells hold approximately 21,000 different genes.

    Genetics is the science of the way traits are passed from parent to offspring. For all forms of life, continuity of the species depends upon the genetic code being passed from parent to offspring. Evolution by natural selection is dependent on traits being heritable. Genetics is very important in human physiology because all attributes of the human body are affected by a person’s genetic code. It can be as simple as eye color, height, or hair color. Or it can be as complex as how well your liver processes toxins, whether you will be prone to heart disease or breast cancer, and whether you will be color blind.

    Genetic inheritance begins at the time of conception. You inherited 23 chromosomes from your mother and 23 from your father. Together they form 22 pairs of autosomal chromosomes and a pair of sex chromosomes (either XX if you are female, or XY if you are male). Homologous chromosomes have the same genes in the same positions, but may have different alleles (varieties) of those genes. There can be many alleles of a gene within a population, but an individual within that population only has two copies and can be homozygous (both copies the same) or heterozygous (the two copies are different) for any given gene.

    The units that determine the inheritance of biological characteristics are
    Figure \(\PageIndex{1}\): Gene pairs enable genetic combinations: A child will inherit half of its genes (one of each of its 23 pairs) from its mother and the other half from its father.

    Key Points

    • A gene is a stretch of DNA that helps to control the development and function of all organs and working systems in the body.
    • Genes are passed from parent to offspring; the combination of these genes affects all aspects of the human body, from eye and hair color to how well the liver can process toxins.
    • A human will inherit 23 chromosomes from its mother and 23 from its father; together, these form 23 pairs of chromosomes that direct the inherited characteristics of the individual.
    • If the two copies of a gene inherited from each parent are the same, that individual is said to be homozygous for the gene; if the two copies inherited from each parent are different, that individual is said to be heterozygous for the gene.

    Key Terms

    • gene: a unit of heredity; the functional units of chromosomes that determine specific characteristics by coding for specific proteins
    • chromosome: a structure in the cell nucleus that contains DNA, histone protein, and other structural proteins
    • genetics: the branch of biology that deals with the transmission and variation of inherited characteristics, in particular chromosomes and DNA

    A gene is the basic physical and functional unit of heredity. Genes are made up of DNA. Some genes act as instructions to make molecules called proteins. However, many genes do not code for proteins. In humans, genes vary in size from a few hundred DNA bases to more than 2 million bases. An international research effort called the Human Genome Project, which worked to determine the sequence of the human genome and identify the genes that it contains, estimated that humans have between 20,000 and 25,000 genes.

    Every person has two copies of each gene, one inherited from each parent. Most genes are the same in all people, but a small number of genes (less than 1 percent of the total) are slightly different between people. Alleles are forms of the same gene with small differences in their sequence of DNA bases. These small differences contribute to each person’s unique physical features.

    Scientists keep track of genes by giving them unique names. Because gene names can be long, genes are also assigned symbols, which are short combinations of letters (and sometimes numbers) that represent an abbreviated version of the gene name. For example, a gene on chromosome 7 that has been associated with cystic fibrosis is called the cystic fibrosis transmembrane conductance regulator; its symbol is CFTR.

    What determines biological inheritance?

    The inheritance of each trait is determined by 'factors' (now known as genes) that are passed onto descendants. Individuals inherit one 'factor' from each parent for each trait. A trait may not show up in an individual but can still be passed onto the next generation.

    What is the unit of inheritance in biology?

    The basic unit of heredity is the gene.

    What is a unit that determines a trait?

    Gene. A segment of a DNA molecule (a sequence of bases) that codes for a particular protein and determines the traits (phenotype) of the individual. A gene is the basic unit of heredity in a living organism.

    What is the unit of inheritance and where is it found?

    the units of inheritance in living organisms are the genes which are the hereditary characters present in an individual. it is present in the chromosomes in the nucleus of a cell.