• Crossing over is initiated
by enzyme endonuclease
which induces nicks
(single strand cuts) in each
chromatids.
• Gaps develop in the region
of nicks by the activity of
another enzyme called
exonuclease.
• The free ends on one side
of the cuts are displaced
from their complementary
strands with the aid of
DNa-unwinding proteins
i.e., enzyme unwindase.
• The displaced strands
then base-pair with the
complementary intact strand
of the other homologue, that
is, the cleaved single strand
of homologue 1 base pairs
with the complementary
intact of homologue 2, and
vice versa.
• Gaps left are later filled by DNa polymerase and joined
together by enzyme ligase.
Diplotene
• The nucleoprotein fusion complex of the synapsed
chromosomes dissolves partially. The homologous
chromosomes separate except in the region of crossing
over. It makes chromatid more distinct and tetrad more
clear. The points of attachment between the homologous
chromosomes after the partial dissolution of nucleoprotein
complex are called chiasmata.
• The number and position of chiasmata varies with the length
of chromosomes and with the species. Chiasma (plural-
chiasmata) formed at the ends of chromosome is called
terminal chiasma and along the length of chromosome is
called interstitial chiasma.
• Diplotene is extended and metabolically active in animal
cells, especially in oocytes because bulk of gametic growth
occurs during this phase. In human oocytes, diplotene stage
last for many years. Suspended diplotene stage is called as
dictyotene stage.
• In amphibian oocytes, chromosomes decondense and get
engaged in rapid rNa synthesis. Lampbrush chromosomes
are actually decondensed diplotene chromosomes.
Diakinesis
• bivalent totally separates and nuclear
Fig.:Diakinesis
membrane disappears.
• During diakinesis, interstitial
chiasma is displaced at the position
of terminal chiasma. This process is
called terminalisation.