PomBase home

Reference - PMID:21920317 - Repositioning of aurora B promoted by chiasmata ensures sister chromatid mono-orientation in meiosis I.

Reference summary

PubMed ID
PMID:21920317
Title
Repositioning of aurora B promoted by chiasmata ensures sister chromatid mono-orientation in meiosis I.
Authors
Sakuno T, Tanaka K, Hauf S, Watanabe Y
Citation
Dev Cell 2011 Sep 13;21(3):534-45
Publication year
2011
Abstract
During meiosis I, kinetochores of sister chromatids are juxtaposed or fused and mono-orient, while homologous chromosomes that are paired by chiasmata (bivalents) have to biorient. In the absence of chiasmata, biorientation of sister chromatids (univalents), which carries a risk of aneuploidy, has been occasionally detected in several species, including humans. We show in fission yeast that biorientation of fused sister kinetochores predominates during early prometaphase I. Without chiasmata, this undesirable biorientation of univalents persists and eventually evades the spindle assembly checkpoint, provoking abnormal anaphase. When univalents are connected by chiasmata or by an artificial tether, this erroneous attachment is converted to monopolar attachment and stabilized. This stabilization is apparently achieved by a chromosome configuration that brings kinetochores to the outer edge of the bivalent, while bringing Aurora B, a destabilizer of kinetochore-microtubule attachment, inward. Our results elucidate how chiasmata favor biorientation of bivalents over that of univalents at meiosis I.

Annotation

GO biological process

GO:0051316 - attachment of meiotic spindle microtubules to kinetochore

Genes:

GO:0031619 - homologous chromosome orientation in meiotic metaphase I

Genes:

GO:0033316 - meiotic spindle assembly checkpoint signaling

Genes:

GO:1904967 - regulation of spindle attachment to meiosis I kinetochore

Genes:

GO cellular component

GO:0000939 - inner kinetochore

Genes:

GO:0000776 - kinetochore

Genes:

GO:0072687 - meiotic spindle

Genes:

Multi-locus phenotype

FYPO:0005641 - abnormal chromosome segregation during meiosis I with premature sister kinetochore separation, lagging chromosomes, and normal chromosome separation

Genes:

Genotypes:

FYPO:0005383 - normal duration of meiosis I

Genes:

Genotypes:

FYPO:0005634 - sister kinetochore dissociation in meiotic metaphase I with equational sister chromatid segregation in meiosis I

Genes:

Genotypes:

FYPO:0005633 - sister kinetochore dissociation in meiotic metaphase I, normal chromosome segregation in meiosis I, and sister chromatid non-disjunction in meiosis II

Genes:

Genotypes:

Single locus phenotype

FYPO:0003177 - abnormal meiotic homologous chromosome biorientation

Genes:

Genotypes:

FYPO:0005642 - abnormal meiotic homologous chromosome biorientation with abnormal kinetochore orientation

Genes:

Genotypes:

FYPO:0000131 - abnormal mitotic spindle elongation

Genes:

Genotypes:

FYPO:0005636 - delayed onset of protein localization from kinetochore to spindle during meiosis I

Genes:

Genotypes:

FYPO:0005512 - increased activation of meiosis I spindle assembly checkpoint

Genes:

Genotypes:

FYPO:0005384 - meiosis I metaphase/anaphase transition delay

Genes:

Genotypes:

FYPO:0002219 - normal chromosome disjunction at meiosis I

Genes:

Genotypes:

FYPO:0004667 - normal meiotic sister chromatid cohesion at centromere

Genes:

Genotypes:

FYPO:0005634 - sister kinetochore dissociation in meiotic metaphase I with equational sister chromatid segregation in meiosis I

Genes:

Genotypes:

FYPO:0005633 - sister kinetochore dissociation in meiotic metaphase I, normal chromosome segregation in meiosis I, and sister chromatid non-disjunction in meiosis II

Genes:

Genotypes: