Death regulator Nedd2-like caspase

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Death regulator Nedd2-like caspase (Dronc)
Animation of the crystal structure of the Dronc caspase zymogen.[1]
Identifiers
OrganismDrosophila melanogaster
SymbolCG8091
Alt. symbolsNc, Nedd2-like caspase, caspase-9
HomoloGene76771
PDB2FP3
UniProtQ9XYF4
Other data
EC numberK20009
Chromosome3L: 9.97 - 9.97 Mb
Search for
StructuresSwiss-model
DomainsInterPro

Death regulator Nedd2-like caspase (Nc, Nedd2-like caspase or Dronc) was firstly identified and characterised in Drosophila in 1999 as a cysteine protease containing an amino-terminal caspase recruitment domain.[2] At first, it was thought of as an effector caspase involved in apoptosis, but subsequent findings have proved that it is, in fact, an initiator caspase with a crucial role in said type of programmed cell death.

Structure[edit]

Caspase Dronc is a Drosophila melanogaster protein codified by the Dronc gene. It belongs to the cysteine-aspartic proteases family, as it is a protease enzyme that takes part in programmed cell death processes. It is composed of beta-sheet structures surrounded by alpha-helices, which is a common feature in the protein family. Caspases are formed by ensembled or single active heterodimers that come from the intra-chain proteolytic cleavage of inactive zymogens. This cleavage is coordinated by a specific initiator caspase (which undergoes adaptor-assisted self-activation) for each effector caspase. A common feature among initiator caspases is the presence of a long amino-terminal domain with intermolecular interaction motifs such as the caspase recruiting domain (CARD).[3]

Five caspases have been identified in Drosophila. Two of these present long prodomains (structural domains of the caspases) and are considered to be initiator caspases (Dronc and DCP-2 / DREDD). The other three (DCP-1, DrICE and DECAY), which have short prodomains, act as effector caspases activated by initiator caspases.[4] The uncleaved Dronc zymogen is only presented as a monomer, while the autocleaved protein forms a homodimer. It is presumed that its autocatalytic cleavage activates the protein by generating a dimerisation in which both monomers stabilise their active sites mutually. Caspase Dronc's active site is located between positions 271 and 318 of the protein sequence.[5]

Genetics[edit]

The Dronc gene is located in the 3L chromosome of the fly, between the 9,968,479 bp and the 9,971,002 bp. It transcripts one single polypeptide and there are 66 reported alleles of the gene. Two mutations have been found in the positions 150 and 184, respectively.[1] The Dronc protein has a length of 450 amino acids and a mass of 51,141 Da.[5]

COMPLETE DRONC SEQUENCE
11 21 31 41
MQPPELEIGM PKRHREHIRK NLNILVEWTN YERLAMECVQ QGILTVQMLR
51 61 71 81 91
NTQDLNGKPF NMDEKDVRVE QHRRLLLKIT QRGPTAYNLL INALRNINCL
101 111 121 131 141
DAAVLLESVD ESDSRPPFIS LNERRTSRKS ADIVDTPSPE ASEGPCVSKL
151 161 171 181 191
RNEPLGALTP YVGVVDGPEV KKSKKIHGGD SAILGTYKMQ SRFNRGVLLM
201 211 221 231 241
VNIMDYPDQN RRRIGAEKDS KSLIHLFQEL NFTIFPYGNV NQDQFFKLLT
251 261 271 281 291
MVTSSSYVQN TECFVMVLMT HGNSVEGKEK VEFCDGSVVD MQKIKDHFQT
301 311 321 331 341
AKCPYLVNKP KVLMFPFCRG DEYDLGHPKN QGNLMEPVYT AQEEKWPDTQ
351 361 371 381 391
TEGIPSPSTN VPSLADTLVC YANTPGYVTH RDLDTGSWYI QKFCQVMADH
401 411 421 431 441
AHDTDLEDIL KKTSEAVGNK RTKKGSMQTG AYDNLGFNKK LYFNPGFFNE

Human orthologs[edit]

Although most human caspases are considered orthologs of caspase Dronc, the one that resembles it the most is Caspase-2. However, Nedd2-like caspase is the functional homolog of mammalian Caspase-9.[6]

Location[edit]

Figure 1. The apoptosome is a ring-like multisubunit complex assembled upon receiving a pro-apoptotic signal. In Drosophila, Dark gathers two bundled rings of eight subunits each. This scaffold attaches Adenosine diphosphate (ADP) and an initiator caspase (Dronc in D. melanogaster), which in turn further advances the signalling cascade by cleaving of the effector caspase(s).[7] Crystal structure of D. melanogaster's apoptosome.[7]

Due to its function and its mostly hydrophilic character, Dronc can be located in the apoptosome, the plasma membrane and the nucleus of the cell. Cells containing this protein have been found in the following structures of the Drosophila melanogaster: extended germ band embryo; eye disc; foregut primordium; germline cyst; and gut section.[8]

Activation[edit]

The activation of caspases is a fundamental step required to execute apoptosis. Initiator caspases, such as Dronc, which is the only initiator caspase in Drosophila melanogaster, are activated through different mechanisms, the main one being autocleavage. Understanding how caspases are activated is a crucial element in order to come up with therapeutic treatments triggering specific caspases. For instance, it has been shown that mice missing or having inactivated caspase-9 present several neurological impairments and have a faulty response to cell damage.[9][10] Just as caspase 9 in mammals, caspase Dronc is a protein that has a caspase activation and recruitment domain (CARD). It is the only Drosophila caspase presenting this domain: this can represent the possibility of establishing a valuable comparison between their activation or inhibition mechanisms.[9][11][12]

Activation[edit]

Autocleavage[edit]

To activate zymogen at first, caspase Dronc autocleaves at residue E352 (Glu352, a glutamic acid residue). Autocleavage at this residue induces dimerization and stabilization of the active site.[2] Autocleavage at E352 results in Pr1, which weighs 40kDa. One study showed that, in Drosophila melanogaster S2 cells, Dronc autocleavage is essential for the zymogen activation. Even though caspase Dronc goes through other processes which will be discussed later, Dronc autocleavage was found to be absolutely necessary to induce apoptosis, whereas other cell cofactors seemed to not be enough to induce activation of Dronc if it had not previously been autocleaved at residue E352.[13] After autocleavage, catalytic activity of Dronc is drastically higher than that of the zymogen.[14] However, these results seem to be contradictory with those of another study conducted in BG2 cells. This study concluded that autocleavage at residue E352, just as autocleavage at other sites such as E143, is not needed for Dronc to activate and, consequently, to induce apoptosis.[2]

Processing by DrICE[edit]

Dronc can also be cleaved by the effector caspase DrICE, which is activated by caspase Dronc itself after autocleavage.[2][13] However, it has also been suggested that caspases other than Dronc could activate DrICE.[15] Even though uncleavable mutations of Dronc may have the ability to process caspase DrICE, it is autocleaved Dronc that processes caspase DrICE in Drosophila melanogaster cells. Cleavage of Dronc by DrICE occurs at residue D135 (Asp135, an aspartic acid residue). At the beginning of apoptosis, full-length Dronc and autocleaved Dronc, Pr1, are present and can be used as a substrate for DrICE processing. Cleavage at residue D135 can therefore result in two products: cleavage of Dronc Pr1 results in fully processed Dronc, whereas cleavage of full Dronc results in Pr2, which weights 36kDa. However, since Dronc Pr1 seems to be the most abundant during early stages of apoptosis, most caspase Dronc ends up being fully processed.[13]

Interaction with apoptosome[edit]

In humans, initiator caspases such as Caspase-2 and Caspase-9 have a prodomain that cleaves caspases to a holoenzyme complex in order to activate the protein. These caspases have a caspase recruitment domain (CARD) that allows them to interact with Apaf-1. The Drosophila melanogaster Apaf-1 homolog, Dark, forms an oligomer with eight Dark chains when dATP is present. This complex is called the apoptosome.[2][16] Dark, just as Apaf-1, has an N-terminal CARD domain that interacts with caspase Dronc, which is incorporated into this protein complex that will induce cell death.[12]

Recruitment of Dronc by Dark seems to facilitate Dronc autocleavage at residue E352. Dark might not be enough on its own to activate caspase Dronc; it has been suggested that other factors could increase the activation of Dronc (and DrICE) through interaction with the apoptosome.[2] However, in Drosophila melanogaster cells, Dark activity is necessary for normal execution of apoptosis.[14]

Inhibition[edit]

Ubiquitylation[edit]

Figure 2. Regulation of Dronc's activity through mono-ubiquitylation. At K78, Diap-1 mono-ubiquitylates Dronc which exists the initiator caspase's CARD domain. Dronc 's association with Dark and thereby apoptosome formation is impeded by said ubiquitylation. It has inhibitory repercussions for both Dronc's apoptotic and non-apoptotic roles, since apoptosome formation is essential for the protease's activation. K78 mono-ubiquitylation may be capable of blocking interactions with some proteins which can have a detrimental impact on Dronc's non-apoptotic functions.

Activation of Dronc is also monitored by ubiquitylation. (see figure 2) Ubiquitylation is a modification that happens after protein translation: in this process, protein ubiquitin conjugates to a lysine residue. However, the exact mechanism of Dronc ubiquitylation remains partially unknown to this day. In Drosophila melanogaster cells, mono-ubiquitylation on residue K78 (located in the CARD domain) is carried in caspase Dronc. Ubiquitylation of this residue of the CARD domain, which interacts with the apoptosome during apoptosis, keeps Dronc from activating in the apoptosome and prevents apoptosis of the cell. Ubiquitylation by E3 ubiquitin ligase activity of Diap-1 negatively regulates Dronc activity.[9] Even a partial decrease in ubiquitylation is already enough to importantly rise Dronc activity. Moreover, it has also been shown that K78 mono-ubiquitylation assumes an inhibitory role in Dronc's non-apoptotic capacities, which may not need its catalytic movement, but still being significant for the endurance of the fruit fly.[12] In Drosophila melanogaster cells, caspase Dronc is ubiquitylated by Diap-1. Similarly, effector caspases Caspase-3 and Caspase-7 are monoubiquitylated by cIAP2 in vitro.[12]

Diap-1[edit]

Inhibitor of Apoptosis Proteins (IAPs) are a family of proteins that act as endogenous inhibitors of apoptosis: they inhibit caspases. Diap-1 is the Drosophila melanogaster IAP that interacts with both Dronc and DrICE through IAP domains.[12] Some studies have found that Diap-1 inhibits and degrades caspase Dronc,[17][18][19][20] and impairment of Diap-1 interaction with Dronc would prevent the caspase from degrading.[13]

Diap-1 regulates caspase activity in Drosophila melanogaster, thus making Dronc activation dependent on removing Diap-1. Diap-1 is the protein that inhibits both Dronc and DrICE, and prevents apoptosis from being executed. Removal of Diap-1 RNAi triggers caspase activation and, thus, apoptosis. Moreover, during apoptosis, removal of Diap-1 facilitates interaction between Dronc and Dark, which supports the fact that Diap-1 is charged of regulating and inhibiting caspase Dronc. In fact, during apoptosis, proteosomal degradation of Diap-1 takes place (and is necessary) right before cleavage and activation of caspases Dronc and DrICE.[2] Finally, binding of Diap-1 seems to not be sufficient for Dronc inhibition; it seems that ubiquitylation the RING domain of Diap-1 is necessary for complete inhibition of Dronc.[12]

Functions[edit]

Caspase Dronc has an essential catalytic activity. It is defined as a cysteine protease (or thiol protease), which means that a nucleophilic cysteine thiol forms a catalytic triad (Cys–His–Asn) at the active site of the enzyme that intercedes in the catalysis.[21] The main function of this kind of endopeptidases is to catalyze the hydrolysis of peptide bonds in order to cleave proteins into smaller fragments (see figure 3).[22] For that reason, Nedd2-like caspase is responsible for the activation of effector caspases. On the other hand, as a caspase, Dronc is fully involved in programmed cell death (PCD) processes, which have repercussions in regulative and reproductive functions of the Drosophila melanogaster.

Apoptotic functions[edit]

Apoptosis is an essential process for the development of multicellular organisms. Its role is to remove excess cells during development (e.g. sculpting the digits of vertebrates), as well as being responsible for detaching damaged, potentially dangerous, cells.[23] Because of its extreme importance, this pathway has been shown to be vastly conserved throughout evolution.[24] One event that is capable of triggering this type of programmed cell death is the activation of the JNK (c-Jun N-terminal kinase) signalling pathway, due to stress caused by chromosomal instability (CIN).[25]

Figure 3. Reaction mechanism of the cysteine protease-mediated cleavage of a peptide bond.

The apoptosis pathway is regulated by caspases, a family of proteases that lead to the disassembling of the cell by cleaving protein targets following an aspartate residue. In response to certain apoptotic stimuli, the inactive caspases zymogens turn into active enzymes that start a cascade of caspases-induced proteolytic cleavage processes which culminate with the DNA decomposition and the cell death.[9] Next, neighbouring cells or macrophages (often called apoptotic bodies) engulf whatever is left of the dwindled cell in order to minimize its effect on the surrounding ones, and at the same time to avoid inducing an immune response in the body. Studies link failure of apoptosis activation with the development of some types of cancer.[26]

Specifically, in the context of the apoptotic signalling cascade, Dronc's role as an initiator caspase consists in the activation of effector caspases such as DrICE or Dcp-1. Nonetheless, Dronc has been found to be a surprisingly efficient catalyst, with a kinetic performance one hundred and eightyfold lesser than that of caspase-9.[27] Hence, akin to caspase 9's behaviour, an adequate enzymatic activity might demand the formation of a holoenzyme complex involving close associations with Dark, Apaf-1's Drosophila ortholog.[28][29]

Comparison of the main apoptotic machinery[edit]

The diagram (figure 4) shows functional homologues of apoptotic proteins (colour-coded correspondence) in Drosophila melanogaster and mammals.

Figure 4. Comparison of the core apoptotic machinery involved in its intrinsic pathways in Drosophila and mammals.

A) Drosophila: In individuals of the Drosophila genus numerous signalling pathways in charge of regulating anti-IAPs Reaper, Hid, and Grim (RHG), Dark scaffold proteins, and Dronc initiator caspases. On the one hand, RHG expression causes the degradation of Diap-1, Inhibitors of apoptosis proteins (IAPs) and the release of Dronc initiator caspases. On the other hand, it allows it to associate with Dark scaffold proteins to form a functional apoptosome and activate the DrICE and Dcp-1 effector caspases. Both pathways are necessary to properly activate caspases and are coordinately regulated. Of note is the existence of the protein from a p35 baculovirus, which has the ability to suppress them, thus blocking the pathway.  

B) Mammals: Among members of the class Mammalia,  the balance between members of the pro- and anti-apoptotic Bcl-2 family is a key factor in the commitment to apoptosis by regulating the release of cytochrome and IAP antagonists of mitochondria. The binding of cyt c to Apaf-1 promotes apoptosome assembly, which in turn groups and activates caspase-9s. In the end, anti-IAPs release the IAPs proteins (mainly XIAPs).

Development (Metamorphosis)[edit]

Apoptosis can be triggered by extrinsic or intrinsic signals. Both of them occur in Drosophila during its development. For example, a higher concentration of ecdysones (common during the metamorphosis) leads cuticle deposition and larval moults, as well as puparium formation and histolysis of larval midgut. This hormone causes head evasion as well as cell death of larval salivary gland. It is thought that ecdysone induced apoptosis is regulated by the Caspase Dronc.[9][30] This protein conducts Rpc- and Grim-induced apoptosis, but not Hid-. Regarding other developmental processes, apoptosis conducts the ratio of stem cell-like neuroblasts in the central nervous system.[31]

Additionally, research shows that through the employment the iRNA (RNA interference) mechanism, budding Drosophila embryos have displayed a striking reduction of cell death processes, thus demonstrating that Dronc is important for programmed cell death during embryogenesis.[32] The outcome of said experiments results lead to believe that D. melanogaster's initiator caspase plays an essential role in mediating PCD.

Accidental Cell Death and Compensatory Proliferation[edit]

Cell death during animal tissues development is rapidly compensated by cell divisions in a process called compensatory proliferation. The developing Drosophila imaginal disk has a very high regenerative capacity that is independent of the size control mechanism that governs the disk.[33] It is not completely known how these phenomena are regulated, but it is thought that dying cells secrete mitogens that activate the reproduction of neighbouring cells, a process that would be regulated by apoptotic signalling pathway (in which Caspase Dronc is involved). This means that if cells were stimulated to undergo apoptosis, and at the same time artificially kept alive (e.g. by overexpressing the inhibitor of effector caspases, p35), neighbouring cells would be led to conduct uncontrollable compensatory proliferation.[34][35][36] The fact that Dronc is insensitive to p35 inhibition has suggested that it could be required for compensatory proliferation, a hypothesis that was demonstrated in 2006.[33]

Non-apoptotic functions[edit]

Promoting DNA damage signalling[edit]

In addition to its role in apoptosis and compensatory proliferation, Caspase Dronc promotes DNA damage signalling by facilitating γH2Av activity, a variation of histone H2Ax whose phosphorylation marks DNA damage and repairs it by recruiting DNA repair machinery. Thus, Dronc would be involved in both DDR and apoptosis depending on its availability and the needs of the organism.[37]

Involvement in genetic pathologies[edit]

Cancer[edit]

Tissue homeostasis can be defined as the maintenance of a balance between cell division and PCD, resulting in the tissue in question maintaining a relatively constant number of cells.[38] In case it gets disturbed, two things could happen. The first would be for the cells to die faster than they can divide, which would result in tissue atrophy. Alternatively, if programmed cell death were blocked in some of the cells, they would not die enough and would end up triggering carcinogenesis in the tissue. For this reason, apoptosis evasion has been identified as a key hallmark of cancer.[39]

As previously mentioned, caspases have a decisive implication in the initiation and execution of apoptosis. Therefore, it is reasonable to think that at low levels they can cause decreased apoptosis and carcinogenesis. Somatic mutations in caspase-3 were detected at fairly low frequencies in certain human cancers, like colon and stomach cancer and non-Hodgkin's lymphoma (NHL).[26] Furthermore, decreased caspase 9 (a human Dronc ortholog) expression has also been linked to 46% of colon cancers.[40]

Alzheimer's disease[edit]

Caspase-2 could have an implication in neurodegenerative disorders such as Alzheimer's disease. Latest evidence has shown that Tau's Caspase-2 cleavage results in the decline of Alzheimer's memory function.[41] Notably, Dronc-dependent Tau cleavage was also shown in an experiment that connected circadian rhythm and Alzheimer's disease.[42] To boot, it was also discovered that Tau expression mediated by the initiator caspase in question could induce a rough eye phenotype due to degeneration of photoreceptor neurons of Drosophila melanogaster.[43]

Oxidative stress and ageing[edit]

An experiment questioning the impact of apoptosis on ageing found that caspase-2-deficient mice displayed shortened life-span and elevated characteristics associated with ageing.[44] Further research has established that caspase-2 plays a role in oxidative stress response, mitochondrial function regulation and metabolic pathways, which may be potential mechanisms through which said caspase regulates ageing.[45] Concurrently, Dronc null mutant flies, also perished within a few days after hatching.[46] In addition, another review has shown that aging flies have raised activated Dronc levels.[42]

References[edit]

  1. ^ a b PDB: 2FP3​; Yan N, Huh JR, Schirf V, Demeler B, Hay BA, Shi Y (March 2006). "Structure and activation mechanism of the Drosophila initiator caspase Dronc". The Journal of Biological Chemistry. 281 (13): 8667–74. doi:10.1074/jbc.M513232200. PMID 16446367. S2CID 15529567.
  2. ^ a b c d e f g Dorstyn L, Colussi PA, Quinn LM, Richardson H, Kumar S (April 1999). "DRONC, an ecdysone-inducible Drosophila caspase". Proceedings of the National Academy of Sciences of the United States of America. 96 (8): 4307–12. Bibcode:1999PNAS...96.4307D. doi:10.1073/pnas.96.8.4307. PMC 16328. PMID 10200258.
  3. ^ "Caspase - an overview | ScienceDirect Topics". www.sciencedirect.com. Retrieved 2020-11-05.
  4. ^ "Fisiologia apoptosis drosophila". www3.uah.es. Archived from the original on 2008-12-02. Retrieved 2020-11-01.
  5. ^ a b "Dronc - Caspase Dronc precursor - Drosophila melanogaster (Fruit fly) - Dronc gene & protein". www.uniprot.org. Retrieved 2020-11-01.
  6. ^ Snipas SJ, Drag M, Stennicke HR, Salvesen GS (May 2008). "Activation mechanism and substrate specificity of the Drosophila initiator caspase DRONC". Cell Death and Differentiation. 15 (5): 938–45. doi:10.1038/cdd.2008.23. PMID 18309328. S2CID 22335875.
  7. ^ a b PDB: 3J9K 3J9K​; Pang Y, Bai XC, Yan C, Hao Q, Chen Z, Wang JW, et al. (February 2015). "Structure of the apoptosome: mechanistic insights into activation of an initiator caspase from Drosophila". Genes & Development. 29 (3): 277–87. doi:10.1101/gad.255877.114. PMC 4318144. PMID 25644603.
  8. ^ "FlyBase Gene Report: Dmel\Dronc". flybase.org. Retrieved 2020-11-01.
  9. ^ a b c d e Waldhuber M, Emoto K, Petritsch C (July 2005). "The Drosophila caspase DRONC is required for metamorphosis and cell death in response to irradiation and developmental signals". Mechanisms of Development. 122 (7–8): 914–27. doi:10.1016/j.mod.2005.04.003. PMID 15922568. S2CID 11991078.
  10. ^ Zheng TS, Hunot S, Kuida K, Flavell RA (November 1999). "Caspase knockouts: matters of life and death". Cell Death and Differentiation. 6 (11): 1043–53. doi:10.1038/sj.cdd.4400593. PMID 10578172. S2CID 1960326.
  11. ^ Kumar S, Doumanis J (November 2000). "The fly caspases". Cell Death and Differentiation. 7 (11): 1039–44. doi:10.1038/sj.cdd.4400756. PMID 11139276. S2CID 24483295.
  12. ^ a b c d e f Kamber Kaya HE, Ditzel M, Meier P, Bergmann A (February 2017). "An inhibitory mono-ubiquitylation of the Drosophila initiator caspase Dronc functions in both apoptotic and non-apoptotic pathways". PLOS Genetics. 13 (2): e1006438. doi:10.1371/journal.pgen.1006438. PMC 5313150. PMID 28207763.
  13. ^ a b c d Muro I, Monser K, Clem RJ (October 2004). "Mechanism of Dronc activation in Drosophila cells". Journal of Cell Science. 117 (Pt 21): 5035–41. doi:10.1242/jcs.01376. PMID 15383617. S2CID 2306221.
  14. ^ a b Yan N, Huh JR, Schirf V, Demeler B, Hay BA, Shi Y (March 2006). "Structure and activation mechanism of the Drosophila initiator caspase Dronc". The Journal of Biological Chemistry. 281 (13): 8667–74. doi:10.1074/jbc.M513232200. PMID 16446367. S2CID 15529567.
  15. ^ Kilpatrick ZE, Cakouros D, Kumar S (March 2005). "Ecdysone-mediated up-regulation of the effector caspase DRICE is required for hormone-dependent apoptosis in Drosophila cells". The Journal of Biological Chemistry. 280 (12): 11981–6. doi:10.1074/jbc.M413971200. PMID 15657059. S2CID 38560973.
  16. ^ Salvesen GS, Abrams JM (April 2004). "Caspase activation - stepping on the gas or releasing the brakes? Lessons from humans and flies". Oncogene. 23 (16): 2774–84. doi:10.1038/sj.onc.1207522. PMID 15077141. S2CID 1757956.
  17. ^ Hawkins CJ, Yoo SJ, Peterson EP, Wang SL, Vernooy SY, Hay BA (September 2000). "The Drosophila caspase DRONC cleaves following glutamate or aspartate and is regulated by DIAP1, HID, and GRIM". The Journal of Biological Chemistry. 275 (35): 27084–93. doi:10.1016/S0021-9258(19)61483-3. PMID 10825159.
  18. ^ Meier P, Silke J, Leevers SJ, Evan GI (February 2000). "The Drosophila caspase DRONC is regulated by DIAP1". The EMBO Journal. 19 (4): 598–611. doi:10.1093/emboj/19.4.598. PMC 305598. PMID 10675329.
  19. ^ Muro I, Hay BA, Clem RJ (December 2002). "The Drosophila DIAP1 protein is required to prevent accumulation of a continuously generated, processed form of the apical caspase DRONC". The Journal of Biological Chemistry. 277 (51): 49644–50. doi:10.1074/jbc.M203464200. PMID 12397080. S2CID 2767113.
  20. ^ Wilson R, Goyal L, Ditzel M, Zachariou A, Baker DA, Agapite J, et al. (June 2002). "The DIAP1 RING finger mediates ubiquitination of Dronc and is indispensable for regulating apoptosis". Nature Cell Biology. 4 (6): 445–50. doi:10.1038/ncb799. PMID 12021771. S2CID 27122989.
  21. ^ "MeSH Browser". meshb.nlm.nih.gov. Retrieved 2020-11-01.
  22. ^ Verma S, Dixit R, Pandey KC (2016-04-25). "Cysteine Proteases: Modes of Activation and Future Prospects as Pharmacological Targets". Frontiers in Pharmacology. 7: 107. doi:10.3389/fphar.2016.00107. PMC 4842899. PMID 27199750.
  23. ^ Mills K, Daish T, Kumar S (June 2005). "The function of the Drosophila caspase DRONC in cell death and development". Cell Cycle. 4 (6): 744–6. doi:10.4161/cc.4.6.1740. PMID 15970694. S2CID 1960475.
  24. ^ Koonin EV, Aravind L (April 2002). "Origin and evolution of eukaryotic apoptosis: the bacterial connection". Cell Death and Differentiation. 9 (4): 394–404. doi:10.1038/sj.cdd.4400991. PMID 11965492. S2CID 5111399.
  25. ^ Ho CY, Li HY (June 2010). "DNA damage during mitosis invokes a JNK-mediated stress response that leads to cell death". Journal of Cellular Biochemistry. 110 (3): 725–31. doi:10.1002/jcb.22583. PMID 20512932. S2CID 11493599.
  26. ^ a b Soung YH, Lee JW, Kim SY, Park WS, Nam SW, Lee JY, et al. (July 2004). "Somatic mutations of CASP3 gene in human cancers". Human Genetics. 115 (2): 112–5. doi:10.1007/s00439-004-1129-3. PMID 15127291. S2CID 12616547.
  27. ^ Kanuka H, Sawamoto K, Inohara N, Matsuno K, Okano H, Miura M (November 1999). "Control of the cell death pathway by Dapaf-1, a Drosophila Apaf-1/CED-4-related caspase activator". Molecular Cell. 4 (5): 757–69. doi:10.1016/S1097-2765(00)80386-X. PMID 10619023.
  28. ^ Rodriguez A, Oliver H, Zou H, Chen P, Wang X, Abrams JM (September 1999). "Dark is a Drosophila homologue of Apaf-1/CED-4 and functions in an evolutionarily conserved death pathway". Nature Cell Biology. 1 (5): 272–9. doi:10.1038/12984. PMID 10559939. S2CID 19619824.
  29. ^ Zhou L, Song Z, Tittel J, Steller H (November 1999). "HAC-1, a Drosophila homolog of APAF-1 and CED-4 functions in developmental and radiation-induced apoptosis". Molecular Cell. 4 (5): 745–55. doi:10.1016/S1097-2765(00)80385-8. PMID 10619022.
  30. ^ Daish TJ, Cakouros D, Kumar S (December 2003). "Distinct promoter regions regulate spatial and temporal expression of the Drosophila caspase dronc". Cell Death and Differentiation. 10 (12): 1348–56. doi:10.1038/sj.cdd.4401312. PMID 12970673. S2CID 44583150.
  31. ^ Harding K, White K (October 2018). "Drosophila as a Model for Developmental Biology: Stem Cell-Fate Decisions in the Developing Nervous System". Journal of Developmental Biology. 6 (4): 25. doi:10.3390/jdb6040025. PMC 6315890. PMID 30347666.
  32. ^ Quinn LM, Dorstyn L, Mills K, Colussi PA, Chen P, Coombe M, et al. (December 2000). "An essential role for the caspase dronc in developmentally programmed cell death in Drosophila". The Journal of Biological Chemistry. 275 (51): 40416–24. doi:10.1074/jbc.M002935200. PMID 10984473. S2CID 13616436.
  33. ^ a b Kondo S, Senoo-Matsuda N, Hiromi Y, Miura M (October 2006). "DRONC coordinates cell death and compensatory proliferation". Molecular and Cellular Biology. 26 (19): 7258–68. doi:10.1128/MCB.00183-06. PMC 1592896. PMID 16980627.
  34. ^ Huh JR, Guo M, Hay BA (July 2004). "Compensatory proliferation induced by cell death in the Drosophila wing disc requires activity of the apical cell death caspase Dronc in a nonapoptotic role". Current Biology. 14 (14): 1262–6. Bibcode:2004CBio...14.1262H. doi:10.1016/j.cub.2004.06.015. PMID 15268856. S2CID 15360684.
  35. ^ Pérez-Garijo A, Martín FA, Morata G (November 2004). "Caspase inhibition during apoptosis causes abnormal signalling and developmental aberrations in Drosophila". Development. 131 (22): 5591–8. doi:10.1242/dev.01432. PMID 15496444. S2CID 32371947.
  36. ^ Ryoo HD, Gorenc T, Steller H (October 2004). "Apoptotic cells can induce compensatory cell proliferation through the JNK and the Wingless signaling pathways". Developmental Cell. 7 (4): 491–501. doi:10.1016/j.devcel.2004.08.019. PMID 15469838.
  37. ^ Khan C, Muliyil S, Ayyub C, Rao BJ (September 2017). "D. melanogaster". Journal of Cell Science. 130 (18): 2984–2995. doi:10.1242/jcs.200782. PMID 28751499. S2CID 33364836.
  38. ^ Lindahl A (2008-01-01). "Chapter 3 - Tissue homeostasis". In van Blitterswijk C, Thomsen P, Lindahl A, Hubbell J (eds.). Tissue Engineering. Burlington: Academic Press. pp. 73–87. ISBN 978-0-12-370869-4. Retrieved 2020-11-04.
  39. ^ Hesketh R (2012). Introduction to Cancer Biology. Cambridge: Cambridge University Press. ISBN 978-1-107-01398-8.
  40. ^ Xu D, Wang C, Shen X, Yu Y, Rui Y, Zhang D, Zhou Z (December 2013). "Apoptotic block in colon cancer cells may be rectified by lentivirus mediated overexpression of caspase-9". Acta Gastro-Enterologica Belgica. 76 (4): 372–80. PMID 24592539.
  41. ^ Zhao X, Kotilinek LA, Smith B, Hlynialuk C, Zahs K, Ramsden M, et al. (November 2016). "Caspase-2 cleavage of tau reversibly impairs memory". Nature Medicine. 22 (11): 1268–1276. doi:10.1038/nm.4199. PMID 27723722. S2CID 3441471.
  42. ^ a b Means JC, Venkatesan A, Gerdes B, Fan JY, Bjes ES, Price JL (May 2015). "Drosophila spaghetti and doubletime link the circadian clock and light to caspases, apoptosis and tauopathy". PLOS Genetics. 11 (5): e1005171. doi:10.1371/journal.pgen.1005171. PMC 4423883. PMID 25951229.
  43. ^ Jackson GR, Wiedau-Pazos M, Sang TK, Wagle N, Brown CA, Massachi S, Geschwind DH (May 2002). "Human wild-type tau interacts with wingless pathway components and produces neurofibrillary pathology in Drosophila". Neuron. 34 (4): 509–19. doi:10.1016/s0896-6273(02)00706-7. PMID 12062036. S2CID 14066600.
  44. ^ Shalini S, Kumar S (2015-01-23). "Caspase-2 and the oxidative stress response". Molecular & Cellular Oncology. 2 (4): e1004956. doi:10.1080/23723556.2015.1004956. PMC 4905344. PMID 27308499.
  45. ^ Zhang Y, Padalecki SS, Chaudhuri AR, De Waal E, Goins BA, Grubbs B, et al. (February 2007). "Caspase-2 deficiency enhances aging-related traits in mice". Mechanisms of Ageing and Development. 128 (2): 213–21. doi:10.1016/j.mad.2006.11.030. PMC 1828128. PMID 17188333.
  46. ^ Xu D, Li Y, Arcaro M, Lackey M, Bergmann A (May 2005). "The CARD-carrying caspase Dronc is essential for most, but not all, developmental cell death in Drosophila". Development. 132 (9): 2125–34. doi:10.1242/dev.01790. PMC 2519871. PMID 15800001.

Further reading[edit]

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