生物
着丝粒
人类人工染色体
染色体
遗传学
DNA
染色体分离
酵母人工染色体
基因组
动细胞
核小体
染色质
核型
分子生物学
中期
作者
Craig W. Gambogi,Jennine M. Dawicki-McKenna,Glennis A. Logsdon,Ben E. Black
标识
DOI:10.1016/j.yexcr.2020.111978
摘要
Centromeres are essential components of all eukaryotic chromosomes, including artificial/synthetic ones built in the laboratory. In humans, centromeres are typically located on repetitive α-satellite DNA, and these sequences are the “major ingredient” in first-generation human artificial chromosomes (HACs). Repetitive centromeric sequences present a major challenge for the design of synthetic mammalian chromosomes because they are difficult to synthesize, assemble, and characterize. Additionally, in most eukaryotes, centromeres are defined epigenetically. Here, we review the role of the genetic and epigenetic contributions to establishing centromere identity, highlighting recent work to hijack the epigenetic machinery to initiate centromere identity on a new generation of HACs built without α-satellite DNA. We also discuss the opportunities and challenges in developing useful unique sequence-based HACs.
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