Mesocricetus auratus      Atypical/PIKK


※ PIKK family introduction

    Phosphatidylinositol-3 kinase-related kinases (PIKKs) belong to atypical protein kinase group, which share little similarity of kinase catalytic domain. PIKKs family contains six members which are involved in responding to various stresses, including DNA damage, blocks in DNA replication, availability of nutrients and errors in mRNA splicing. The protein kinase domain of PIKKS, located in C-terminus, is always flanked by two conserved domain, known as FAT and FATC domain, which may interact and participate in kinase regulation (1). ATM, one of family member, is involved in responding to a specific type of DNA damage, such as DNA double strand breaks, and controls the cell-cycle progression by phosphorylates multiple substrates including p53 and Chk2. In addition, ATM also locates in cytoplasmic especially in neuronal or neuron-like cells (2). Ataxia telangiectasia and Rad3-related protein (ATR) acts as a DNA damage sensor. Activated by DNA lesions including base adducts, crosslinks, DSBs, and compounds that directly promote replication stress such as hydroxyurea and aphidicolin and phosphorylates multiple substrates to control the DNA replication and mitosis (3). mTOR is a serine/threonine protein kinase which is a central regulator of cellular metabolism, growth and survival in response to hormones, growth factors, nutrients, energy and stress signals. mTOR is regulated by dynamic changes in cellular localization (3). Transformation/transcription domain-associated protein (TRRAP) is also structurally related to the PIKK family. TRRAP proteins (Tra1 in budding yeast) are common components of many histone acetyltransferase (HAT) complexes, and mediate a variety of cellular processes by recruiting HAT complexes to chromatin (4).

Reference
1. Lempiainen, H. and Halazonetis, T.D. (2009) Emerging common themes in regulation of PIKKs and PI3Ks. EMBO J, 28, 3067-3073. PMID: 19779456
2. Yang, D.Q., Halaby, M.J., Li, Y., Hibma, J.C. and Burn, P. (2011) Cytoplasmic ATM protein kinase: an emerging therapeutic target for diabetes, cancer and neuronal degeneration. Drug Discov Today, 16, 332-338. PMID: 21315178
3. Lovejoy, C.A. and Cortez, D. (2009) Common mechanisms of PIKK regulation. DNA Repair (Amst), 8, 1004-1008. PMID: 19464237
4. Kanoh, J. and Yanagida, M. (2007) Tel2: a common partner of PIK-related kinases and a link between DNA checkpoint and nutritional response? Genes Cells, 12, 1301-1304. PMID: 18076567


There are 15 genes.  Reviewed (0 or Unreviewed (15

No.StatusiEKPD IDEnsemble Gene IDUniProt AccessionGene Name
1
iEKPD-Mea-0189
ENSMAUG00000011714.1
A0A1U8BXN1
Atm
2
iEKPD-Mea-0237
ENSMAUG00000013539.1
A0A1U8CDB6
Atr
3
iEKPD-Mea-0284
ENSMAUG00000015520.1
A0A1U7R1Y1
Mtor
4
iEKPD-Mea-g008
ENSMAUG00000009972.1
A0A1U7QYW6
Pi4ka
5
iEKPD-Mea-0308
ENSMAUG00000016696.1
A0A1U7RCL1
Pi4kb
6
iEKPD-Mea-0131
ENSMAUG00000009052.1
A0A1U7QYM2
Pik3c2a
7
iEKPD-Mea-g001
ENSMAUG00000021709.1
A0A1U8BVL5
Pik3c2b
8
iEKPD-Mea-g004
ENSMAUG00000014870.1
A0A1U8C5A1
Pik3c2g
9
iEKPD-Mea-0126
ENSMAUG00000008849.1
A0A1U8CKK8
Pik3c3
10
iEKPD-Mea-0390
ENSMAUG00000019874.1
A0A1U8BMD4
Pik3ca
11
iEKPD-Mea-0095
ENSMAUG00000006981.1
A0A1U7Q7Q6
Pik3cb
12
iEKPD-Mea-0030
ENSMAUG00000001319.1
A0A1U8C7V2
Pik3cd
13
iEKPD-Mea-0014
ENSMAUG00000000671.1
A0A1U8CBT5
Pik3cg
14
iEKPD-Mea-0231
ENSMAUG00000013266.1
A0A1U8C8W3
Prkdc
15
iEKPD-Mea-0292
ENSMAUG00000015855.1
A0A1U8C8X8
Trrap