Suppressor of Variegation 3-9 Homolog 2 (Drosophila) Proteins (SUV39H2)

Human Suppressor of Variegation 3-9 Homolog 2 (Drosophila) (SUV39H2) interaction partners

1. Our finding unveils a novel autoregulatory mechanism of SUV39H2 through lysine automethylation

2. Our data show that the differential expression of SUV39H1 (show SUV39H1 Proteins) and SUV39H2 is associated with genomic instability and that the modulation of these HMTases can be an attractive approach to prevent CLL evolution

3. SUV39H2 functioned cooperatively with MAGE-A11 to increase androgen-dependent AR transcriptional activity.

4. histone H3 (show HIST3H3 Proteins) lysine 9 methylation reduction, which may be due to the downregulation of methyltransferase SUV39H2 and the upregulation of demethylase (show MBD2 Proteins) KDM4C (show KDM4C Proteins), was found in CD4 (show CD4 Proteins)(+) T lymphocytes of Latent autoimmune diabetes in adults patients

5. data cannot finally exclude H2AX (show H2AFX Proteins) methylation of SUV39H2 in cells, additional experimental evidence is required to validate this claim.

6. Our results reveal the regulatory mechanism of LSD1 (show KDM1A Proteins) protein through its lysine methylation by SUV39H2 in human cancer cells

7. We also demonstrate that the N324K mutant in the SET domain of SUV39H2 that has been shown to cause an inherited nasal skin disease in Labrador Retrievers renders SUV39H2 inactive

8. Expression of JHDM2A (show KDM3A Proteins) was significantly increased but HDAC2 (show HDAC2 Proteins), HDAC7 (show HDAC7 Proteins), and SUV39H2 were significantly down-regulated in Systemic Sclerosis B cells relative to controls

9. genetic association studies in a Finnish population with type I diabetes: The minor T allele of exonic SNP rs17353856 in SUV39H2 is associated with diabetic retinopathy (in a larger meta-analysis); thus an genetic variation may be protective.

10. findings suggest that Suv39H1 (show SUV39H1 Proteins) and Suv39H2 are key hypoxia-induced methyltransferases; their decline in fetal lung during late gestation is critical for epigenetic changes resulting in the developmental induction of SP-A

Mouse (Murine) Suppressor of Variegation 3-9 Homolog 2 (Drosophila) (SUV39H2) interaction partners

1. The authors show here that the mouse Suv39h2 enzyme differs from Suv39h1 (show SUV39H1 Proteins) by containing an N-terminal basic domain that facilitates retention at mitotic chromatin and provides an additional affinity for major satellite repeat RNA.

2. Data indicate that histone methyltransferase Suv39h2 expression is up-regulated in the liver in liver steatosis.

3. Repeat-associated, Suv39h (show SUV39H1 Proteins)-dependent H3K9me3 displays a dynamic distribution that differs in the epigenome of pluripotent versus more committed cells.

4. ESET (show SETDB1 Proteins) histone methyltransferase can form a large, multi-protein complex(es) with mSin3A/B co-repressors and HDAC1 (show HDAC1 Proteins)/2 that participates in multiple pathways of transcriptional repression.

5. Taken together, the results indicate epigenetic regulation of telomere length in mammals by Suv39h1 (show SUV39H1 Proteins) and Suv39h2.

Pig (Porcine) Suppressor of Variegation 3-9 Homolog 2 (Drosophila) (SUV39H2) interaction partners

1. Knockdown of SUV39H1 (show SUV39H1 Proteins) and SUV39H2 in embryonic stem-like cells and embryonic fibroblasts increases telomere length.