HDAC1 |
– |
Embryo lethality between E9.5-E10.5 |
Hdac1ZP3–Cre: no phenotype |
Leboeuf et al., 2010; Montgomery et al., 2007; Ma et al., 2012
|
|
|
|
Hdac1/Hdac2ZP3–Cre: infertility due to oocyte development arresting at the secondary follicle stage |
|
HDAC2 |
– |
Embryonic and postnatal lethality |
Hdac2ZP3–Cre: reduced fertility but the follicular development is normal |
|
HDAC3 |
Knock down of Hdac3 in oocytes caused pindle/chromo some organization failure. |
Embryonic death at or around the time of gastrulation |
Hdac3Foxl2–ERT2–Cre: promotes the maturation of oocytes independent of LH |
Bhaskara et al., 2008; Li et al., 2017; Wang et al., 2019
|
|
Using HDAC3 inhibitor promotes the maturation of oocytes independent of LH |
|
|
|
HDAC6 |
Inhibition by TubA: the maturational progression and meiotic apparatus assembly in mouse oocytes, and the oocytes failed to extrude the first polar body |
Viable and fertile |
– |
Zhang et al., 2008; Bobrowska et al., 2011; Zhou et al., 2017; Sui et al., 2020a
|
HDAC8 |
knockdown by si-RNA or drug inhibition with its selective inhibitor PCI-34051: spindle defects and chromosome misalignment during oocyte meiotic maturation, accompanied by impaired kinetochore-microtubule attachments |
Death within 4–6 h of birth from brain hemorrhaging |
Hdac8Vasa–Cre: females were subfertile. Hdac8ZP3–Cre: oogenesis and folliculogenesis appeared normal and mice were fertile. |
Zhang K. et al., 2017; Vijay Pratap et al., 2019
|
HDAC11 |
Inhibition of HDAC11 with its selective inhibitor JB3-22: interrupted mouse oocytes meiosis progress, abnormal spindle organization and misaligned chromosomes, impaired kinetochore-microtubule attachment and spindle assembly checkpoint function |
Viable |
– |
Cheng et al., 2014; Sui et al., 2020b
|
SIRT1 |
Activation of SIRT1 by resveratrol in vitro improves oocyte quality and embryo development. Inhibition of SIRT1 results in increased ROS production and abnormal MII plates in mouse oocytes |
Embryonic and fetal lethality |
– |
Liu et al., 2013; Di Emidio et al., 2014; Takeo et al., 2014; Wang et al., 2014; Itami et al., 2015; Li et al., 2016; Khan et al., 2017
|
SIRT2 |
Inhibitor and Knockdown: the progression of oocyte development was blocked |
Viable |
– |
Zhang L. et al., 2014; Riepsamen et al., 2015
|
SIRT3 |
Overexpression of Sirt3 reduces the spindle defects and chromosome misalignment in oocytes |
Viable |
– |
Lombard et al., 2007; Zhang L. et al., 2015
|
SIRT6 |
Depleted Sirt6 results in disruption of spindle morphology and chromosome alignment in oocytes |
Postnatal lethality |
– |
Mostoslavsky et al., 2006; Han et al., 2015
|