Chromosomes and Inheritance
The physical basis of Mendel's inheritance theory is found in chromosomes—threadlike structures in cell nuclei that carry our genetic information. Humans have 23 pairs of chromosomes, with each pair containing matching genes (alleles) at the same locations.
Chromosomes are made of DNA (deoxyribonucleic acid), a double-stranded molecule composed of four nucleotide bases: adenine, thymine, guanine, and cytosine. The specific sequence of these bases forms the genetic code that determines our traits.
DNA replication is crucial for cell division but isn't always perfect. Errors can lead to conditions like Down Syndrome (an extra chromosome) or mutations (alterations in individual genes). Most mutations disappear from the gene pool within a few generations if they reduce an organism's fitness.
Meiosis is the specialized cell division process that produces gametes (egg and sperm cells). During meiosis, chromosome pairs separate, with one chromosome from each pair going to each new cell. This halves the chromosome number (to 23 in humans), which is restored to the full complement when sperm and egg unite during fertilization.
Two important developmental concepts are:
- Ontogeny: an individual's development over their lifetime
- Phylogeny: the evolutionary development of species over time
Understanding heritability is complex—it's not simply about individual development but about population patterns. Our traits result from complex interactions between our genetic inheritance and our environment, not just one or the other.
Remember: Heritability refers to population-level variation, not individual destiny. A highly heritable trait doesn't mean environment plays no role—it means genetic differences explain much of the variation seen across a population under specific environmental conditions.