Molecular insights on cytochrome c and nucleotide regulation of apoptosome function and its implication in cancer.

Molecular insights on cytochrome c and nucleotide regulation of apoptosome function and its implication in cancer.
复制标题

DOI:
10.1016/j.bbamcr.2019.118573
复制
发表时间:
2020-01
期刊:
Biochimica et biophysica acta. Molecular cell research
影响因子:
--
通讯作者:
Chandra D
Chandra D
中科院分区:
其他
文献类型:
--
作者:
Yadav N;Gogada R;O'Malley J;Gundampati RK;Jayanthi S;Hashmi S;Lella R;Zhang D;Wang J;Kumar R;Suresh Kumar TK;Chandra D

文献摘要

参考文献

被引文献

相似文献

Cytochrome c (Cyt c) released from mitochondria interacts with Apaf-1 to form the heptameric apoptosome, which initiates the caspase cascade to execute apoptosis. Although lysine residue at 72 (K72) of Cyt c plays an important role in the Cyt c-Apaf-1 interaction, the underlying mechanism of interaction between Cyt c and Apaf-1 is still not clearly defined. Here we identified multiple lysine residues including K72, which are also known to interact with ATP, to play a key role in Cyt c-Apaf-1 interaction. Mutation of these lysine residues abrogates the apoptosome formation causing inhibition of caspase activation. Using in-silico molecular docking, we have identified Cyt c-binding interface on Apaf-1. Although mutant Cyt c shows higher affinity for Apaf-1, the presence of Cyt c-WT restores the apoptosome activity. ATP addition modulates only mutant Cyt c binding to Apaf-1 but not WT Cyt c binding to Apaf-1. Using TCGA and cBioPortal, we identified multiple mutations in both Apaf-1 and Cyt c that are predicted to interfere with apoptosome assembly. We also demonstrate that transcript levels of various enzymes involved with dATP or ATP synthesis are increased in various cancers. Silencing of nucleotide metabolizing enzymes such as ribonucleotide reductase subunit M1 (RRM1) and ATP-producing glycolytic enzymes PKM2 attenuated ATP production and enhanced caspase activation. These findings suggest important role for lysine residues of Cyt c and nucleotides in the regulation of apoptosome-dependent apoptotic cell death as well as demonstrate how these mutations and nucleotides may have a pivotal role in human diseases such as cancer.
DOI: 10.1016/j.cell.2006.05.026
发表时间: 2006-06-30
期刊: CELL
影响因子: 64.5
作者:
Chandra, Dhyan;Bratton, Shawn B.;Tang, Dean G.
通讯作者: Tang, Dean G.
DOI: 10.1126/scisignal.2004088
发表时间: 2013-04-02
期刊: Science signaling
影响因子: 7.3
作者:
Gao J;Aksoy BA;Dogrusoz U;Dresdner G;Gross B;Sumer SO;Sun Y;Jacobsen A;Sinha R;Larsson E;Cerami E;Sander C;Schultz N
通讯作者: Schultz N
DOI: 10.1074/jbc.m110.202440
发表时间: 2011-08-19
影响因子: 4.8
作者:
Gogada, Raghu;Prabhu, Varun;Chandra, Dhyan
通讯作者: Chandra, Dhyan
DOI: 10.1074/jbc.m107419200
发表时间: 2001-11-09
影响因子: 4.8
作者:
Cain, K;Langlais, C;Cohen, GM
通讯作者: Cohen, GM
DOI: 10.1016/j.molcel.2006.12.013
发表时间: 2007-01-26
期刊: MOLECULAR CELL
影响因子: 16
作者:
Bao, Qing;Lu, Wenyun;Shi, Yigong
通讯作者: Shi, Yigong