Schiller Martin R
Nevada Institute of Personalized Medicine and School of Life Sciences, University of Nevada, 4505 Maryland Pkwy, Las Vegas, Nevada 89154-4004.
Heligenics Inc., 10530 Discovery Dr., Las Vegas, Nevada 89135.
ArXiv. 2025 Jun 19:arXiv:2506.16374v1.
This paper proposes an extension of the traditional Central Dogma of molecular biology to a more dynamic model termed the Central Dogma Cycle (CDC) and a broader network called the Central Dogma Cyclic Network (CDCN). While the Central Dogma is necessary for genetic information flow, it is not sufficient to fully explain cellular memory and information management. The CDC incorporates additional well-established steps, including protein folding and protein networking, highlighting the cyclical nature of information flow in cells. This cyclic architecture is proposed as a key mechanism for cellular memory, drawing analogies to memory functions in computers, such as input, read, write, execute, and erase. The interconnected cycles within the CDCN, including metabolic cycles and signaling pathways, are suggested to function akin to latches in computer memory, contributing to the storage and processing of cellular information beyond nucleic acid sequences. Understanding cellular memory through this cyclic network model offers a new perspective on heredity, cell processes, and the potential disruptions in disease pathology.
本文提出将传统的分子生物学中心法则扩展为一个更具动态性的模型,称为中心法则循环(CDC),以及一个更广泛的网络,称为中心法则循环网络(CDCN)。虽然中心法则对于遗传信息流动是必要的,但它不足以完全解释细胞记忆和信息管理。CDC纳入了其他已确立的步骤,包括蛋白质折叠和蛋白质网络,突出了细胞中信息流的循环性质。这种循环架构被认为是细胞记忆的关键机制,可类比于计算机中的记忆功能,如输入、读取、写入、执行和擦除。CDCN内相互关联的循环,包括代谢循环和信号通路,被认为类似于计算机内存中的锁存器,有助于细胞信息的存储和处理,而不仅仅是核酸序列。通过这个循环网络模型理解细胞记忆,为遗传、细胞过程以及疾病病理学中的潜在破坏提供了新的视角。