登革病毒颗粒的组装与释放
中文名称
通路描述
新合成的登革病毒(DENV)正链 RNA (+ssRNA) 基因组在内质网(ER)中被包装进病毒颗粒,并与结构病毒蛋白 C、prM 和 E 结合(见 Rodenhuis Zybert 等,2010)。 immature 病毒颗粒通过高尔基体转运至分泌囊泡,其中 prM 被切割形成成熟病毒颗粒。在成熟病毒颗粒中,E 蛋白以 90 个头尾取向的 E:M 异二聚体二聚体形式组织,每三个二聚体几乎平行排列并朝向病毒表面,形成平滑的“鱼骨状”构型(E:M:M:E;见 Rodenhuis-Zybert 等,2010)。每个二十面体不对称单元中存在三个化学环境不同的 E:M:M:E 四面体,因此可能在感染的不同阶段发挥不同的作用(见 Rodenhuis-Zybert 等,2010;Pierson & Diamond,2012;Apte-Sengupta 等,2014)。成熟病毒颗粒通过胞吐作用从细胞释放。
英文描述
Processing of Capped Intron-Containing Pre-mRNA Co-transcriptional pre-mRNA splicing is not obligatory. Pre-mRNA splicing begins co-transcriptionally and often continues post-transcriptionally. Human genes contain an average of nine introns per gene, which cannot serve as splicing substrates until both 5' and 3' ends of each intron are synthesized. Thus the time that it takes for pol II to synthesize each intron defines a minimal time and distance along the gene in which splicing factors can be recruited. The time that it takes for pol II to reach the end of the gene defines the maximal time in which splicing could occur co-transcriptionally. Thus, the kinetics of transcription can affect the kinetics of splicing.Any covalent change in a primary (nascent) mRNA transcript is mRNA Processing. For successful gene expression, the primary mRNA transcript needs to be converted to a mature mRNA prior to its translation into polypeptide. Eucaryotic mRNAs undergo a series of complex processing reactions; these begin on nascent transcripts as soon as a few ribonucleotides have been synthesized during transcription by RNA Polymerase II, through the export of the mature mRNA to the cytoplasm, and culminate with mRNA turnover in the cytoplasm.
所含基因
52 个基因
FUS
GTF2F1
GTF2F2
HNRNPA1
HNRNPA2B1
HNRNPA3
HNRNPC
HNRNPD
HNRNPF
HNRNPH1
HNRNPH2
HNRNPK
HNRNPL
HNRNPM
HNRNPR
HNRNPU
METTL14
METTL3
NCBP1
NCBP2
PCBP1
PCBP2
POLR2B
POLR2C
POLR2D
POLR2E
POLR2F
POLR2G
POLR2H
POLR2I
POLR2J
POLR2K
POLR2L
PTBP1
RBM10
RBMX
S5
SRSF1
SRSF10
SRSF11
SRSF12
SRSF2
SRSF3
SRSF4
SRSF5
SRSF6
SRSF7
SRSF8
SRSF9
TRA2B
WTAP
YBX1