TY - JOUR
T1 - Distinct prophase arrest mechanisms in human male meiosis
AU - Jan, Sabrina Z.
AU - Jongejan, Aldo
AU - Korver, Cindy M.
AU - van Daalen, Saskia K. M.
AU - van Pelt, Ans M. M.
AU - Repping, Sjoerd
AU - Hamer, Geert
PY - 2018
Y1 - 2018
N2 - To prevent chromosomal aberrations being transmitted to the offspring, strict meiotic checkpoints are in place to remove aberrant spermatocytes. However, in about 1% of males these checkpoints cause complete meiotic arrest leading to azoospermia and subsequent infertility. Here, we unravel two clearly distinct meiotic arrest mechanisms that occur during prophase of human male meiosis. Type I arrested spermatocytes display severe asynapsis of the homologous chromosomes, disturbed XY-body formation and increased expression of the Y chromosome-encoded gene ZFY and seem to activate a DNA damage pathway leading to induction of p63, possibly causing spermatocyte apoptosis. Type II arrested spermatocytes display normal chromosome synapsis, normal XY-body morphology and meiotic crossover formation but have a lowered expression of several cell cycle regulating genes and fail to silence the X chromosome-encoded gene ZFX. Discovery and understanding of these meiotic arrest mechanisms increases our knowledge of how genomic stability is guarded during human germ cell development.
AB - To prevent chromosomal aberrations being transmitted to the offspring, strict meiotic checkpoints are in place to remove aberrant spermatocytes. However, in about 1% of males these checkpoints cause complete meiotic arrest leading to azoospermia and subsequent infertility. Here, we unravel two clearly distinct meiotic arrest mechanisms that occur during prophase of human male meiosis. Type I arrested spermatocytes display severe asynapsis of the homologous chromosomes, disturbed XY-body formation and increased expression of the Y chromosome-encoded gene ZFY and seem to activate a DNA damage pathway leading to induction of p63, possibly causing spermatocyte apoptosis. Type II arrested spermatocytes display normal chromosome synapsis, normal XY-body morphology and meiotic crossover formation but have a lowered expression of several cell cycle regulating genes and fail to silence the X chromosome-encoded gene ZFX. Discovery and understanding of these meiotic arrest mechanisms increases our knowledge of how genomic stability is guarded during human germ cell development.
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85047471913&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/29540502
U2 - https://doi.org/10.1242/dev.160614
DO - https://doi.org/10.1242/dev.160614
M3 - Article
C2 - 29540502
SN - 0950-1991
VL - 145
JO - Development (Cambridge, England)
JF - Development (Cambridge, England)
IS - 16
M1 - dev160614
ER -