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Chromosomal Mutations or Aberrations: Translocation

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Estimated time: 9 minutes
CISCE: Class 12

Definition: Translocation

Translocation is a chromosomal mutation in which a segment of one chromosome is transferred to a non-homologous chromosome, changing the position of genes without altering their number.

 
CISCE: Class 12

Translocation

  • Structural aberration (change in chromosome structure, not number).
  • Involves breakage of a chromosome segment.
  • Segment reattaches to a different chromosome or a new locus.
  • Leads to rearrangement of genes and may disturb normal inheritance or fertility.
CISCE: Class 12

Types of Translocation

Translocation Type Mechanism
Simple Translocation A broken segment attaches to one end of a non-homologous chromosome.
Shift Translocation A broken segment is inserted into a non-homologous chromosome.
Reciprocal Translocation Two non-homologous chromosomes mutually exchange broken parts (the most common type).

CISCE: Class 12

Effects and Significance

  • Gene position changes – may alter gene expression.
  • Abnormal pairing and segregation during meiosis.
  • Some gametes may receive unbalanced genetic material.
  • Reduced number of viable gametes → partial sterility possible.
CISCE: Class 12

Key Points:

  • Translocation is a structural chromosomal mutation where a piece of one chromosome breaks and attaches to a different, usually non-homologous, chromosome.
  • It causes rearrangement of genes and chromosome sequence, with balanced forms often keeping overall DNA amount similar.
  • Major types are simple, shift/insertion, and reciprocal translocation, where reciprocal involves segment exchange between non-homologous chromosomes.
  • Translocation can disturb meiosis, produce unbalanced gametes, and is linked to problems like partial infertility and certain genetic disorders or cancers.

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