Skip to content
NCERT Exemplar · Q44

Q.How do genes and chromosomes share similarity from the point of view of genetical studies?

Odisha ChseShort· 2mImportance★★★★★
71% · 60/85 Questions
🔒 Locked · start free trial →

You're viewing a preview — the full solution, concept, methods & PYQ mapping are locked.

Start your 14-day free trial to unlock the full solution →

Genes and chromosomes behave as paired units that segregate during gamete formation and assort independently, revealing their parallel behaviour in inheritance — a connection Morgan's fruit fly experiments made visible.

When Mendel worked out his laws of inheritance in the 1860s, he had no idea what a gene physically was. He spoke of "factors" that controlled traits, factors that came in pairs, separated during gamete formation, and recombined in offspring. Decades later, when chromosomes were observed under the microscope, biologists noticed something striking: chromosomes also came in pairs, separated during meiosis, and recombined at fertilization. The parallel was too neat to ignore.

The conceptual breakthrough came when scientists realized that genes and chromosomes share fundamental similarities in their behaviour during inheritance. Both exist as pairs in diploid organisms — each gene has two alleles (one from each parent), and each chromosome has a homologous partner. During gamete formation, both separate so that each gamete receives only one member of the pair. This is Mendel's law of segregation, and it mirrors exactly what chromosomes do during meiosis.

The second similarity lies in independent behaviour. Mendel's law of independent assortment states that different genes sort independently into gametes. Chromosomes, too, assort independently during meiosis — the way one pair of homologous chromosomes separates has no influence on how another pair separates. This parallelism suggested that genes might actually reside on chromosomes, that the abstract "factors" Mendel described were physical entities carried by these thread-like structures.

Note

The term "chromosome" itself means "coloured body" — early microscopists named them for the way they absorbed dyes and became visible under the lens. But their functional significance remained mysterious until the gene-chromosome connection was made.

Thomas Hunt Morgan's experiments with the fruit fly Drosophila melanogaster in the early 1900s provided the decisive evidence. Morgan discovered sex-linked inheritance — traits like white eye colour in flies that were inherited differently in males and females. He traced this pattern to the X chromosome. Here was direct proof: a specific gene (for eye colour) was physically located on a specific chromosome (the X). The gene and the chromosome moved together through generations because the gene was part of the chromosome.

Morgan went further. He found that genes located on the same chromosome did not always assort independently — they showed linkage, staying together more often than Mendel's law would predict. But occasionally they did separate, through a process called recombination or crossing over. The closer two genes were on a chromosome, the less likely they were to be separated. This allowed Morgan and his students to map genes along the length of chromosomes, proving beyond doubt that genes are arranged linearly on chromosomes like beads on a string. …

Unlock everything free for 14 days

  • Full step-by-step solutions
  • Concept-first explanations
  • Methods, shortcuts & mistakes
  • PYQ mapping + timed mock tests

Full access for 14 days. No credit card required.