Incell biology, aparaspeckle is an irregularly shaped compartment of thecell, approximately 0.2-1μm in size,^[1] found in thenucleus'interchromatin space.^[2] First documented inHeLa cells, where there are generally 10-30 per nucleus,^[3] Paraspeckles are now known to also exist in all humanprimary cells, transformed cell lines and tissue sections.^[4] Their name is derived from their distribution in the nucleus; the "para" is short for parallel and the "speckle" refers to the splicing speckles to which they are always in close proximity.^[3] Their function is still not fully understood, but they are thought to regulate gene expression by sequestrating proteins or mRNAs with inverted repeats in their 3′ UTRs.^[5][6]

Paraspeckles are organised into core-shell spheroidal structures; seven proteins on a scaffold oflncRNANEAT1 (the 23kb isoform termed NEAT1_2 or NEAT1v2).^[8] In 2016, West et al. proposed the currently accepted model for Paraspeckles. This was based on their current findings using super-resolution microscopy.^[7] Their models state that theNEAT1_2 scaffold folds into a V-shaped unit. Many of these units then are assembled into a core-shell spheroid by FUS proteins. Core proteinsSFPQ,NONO and PSPC1 tightly associate to the assembled structure. Finally, the shell forms, composed of partially co-localised TDP43 proteins. Due to the integral nature of NEAT1 to paraspeckles assembly, assembly is thought to occur in close proximity toNEAT1 transcription sites.^[8]

It has been noted that Paraspeckles have a great deal of commonality both in features and structures with cytoplasmicstress granules, another type of membrane-less organelle. This conclusion arose from the fact that both contain common component proteins,^[9] become more abundant with stress, seem to function through sequestering other proteins and both have distinct core or shell regions with predictable localised molecules.^[9]

Paraspeckles are dynamic structures that are altered in response to changes in cellular metabolic activity. They are transcription-dependent.^[2] All five of the proposed protein components haveRNA recognition motifs (RRMs)^[3] and, in the absence ofRNA polymerase IItranscription, the Paraspeckle disappears and all of its associated proponents form a crescent shaped perinucleolar cap in the nucleolus. This phenomenon is demonstrated during the cell cycle. In the cell cycle, Paraspeckles are present duringinterphase and during all ofmitosis except fortelophase because, when the two daughter nuclei are formed, there is no RNA Pol II transcription so the protein components instead form aperinucleolar cap. The localization patterns were also duplicated in experiments using transcriptioninhibiting drugs.^[4]

The role of the Paraspeckle is as of yet not fully understood. It has been suggested that the activity of NONO (a.k.a. p54nrb), a protein component, is dependent on its localisation within the nucleus.^[4] Thus, one explanation of the Paraspeckle's function is that it provides ordered localisation of its component proteins and to thereby help direct their activity. In turn, this is believed to give the Paraspeckle a regulatory function overtranscription.^[10] Also, a meta-analysis by Fox et al. (2018)^[9] links the Paraspeckle's regulation to its ability to sequester or steal component proteins andRNAs. This causes other nuclear compartments to be depleted. The current research into the Paraspeckle's function is mainly targeted towards the roles of several of its components to indicate larger cellular use, this page mainly focuses on the roles of Paraspeckle proteins and NEAT1.

The main insight into their physiological function is their location. Prominent Paraspeckles are only found in a subpopulation of cells in murine tissues, e.g.luteal cells or cells at the tip of the gutepithelium.^[9] Hence, based on location Paraspeckles are thought to play a role in cancer regulation, reproduction and viral management.

One focus has been the Paraspeckle's role in cancer and cell stress scenarios. Wang, Z, Li K, Huang, W (2019),^[11] records that quantities of NEAT1 and thus Paraspeckles are increased in digestive system tumours and respiratory cancers. Furthermore, that expression of NEAT1 is associated with tumour size, stage of cancer, ability to spread and overall patient survival. Whilst, failure to regulate NEAT1 production has been linked to non-cancerous diseases, such as neurodegenerative diseases likeParkinson's orAlzheimer's.^[11] However, the function of NEAT1 and Paraspeckles is not always positive, it has been proven that they enhance themalignancy andstemness of breast tumours by increasing the expression of theWNT4 gene.^[4]

NEAT1 also affects pregnancy and fertility chances, especially in femalemammals whose luteal cells are regulated by Paraspeckles.^[10] This can cause malformation or potential no formation of thecorpus luteum leading to infertility, smaller litters, and fewer viable pregnancies. In a study by Chai Y, Liu J, Zhang Z, Liu L (2016),^[9] knockout mice (no NEAT1) exhibited malfunctions in epithelial cell proliferation, causing mothers to lactate poorly and reduced litter survival even further. Interestingly these knockout mice exhibit the stochastic effect; the corpus luteum will form in some, but not in all.^[9] This reinforces the fact that Paraspeckles are inducible by cell stress and that environmental triggers have an impact.

From a viral aspect, NEAT1 levels have an observable impact on infections within cells with many different RNA viruses, includingJapanese encephalitis,rabies,^[11]HIV,^[11][12]influenza,^[13] andHantaan,^[14] as well as the DNA-encodedherpes simplex virus.^[15] Wang, Z, Li K, Huang, W (2019)^[11] suggest NEAT1_2/Paraspeckles act as a promoter to cell defence triggering and aiding the cellular defence mechanism.

From the molecular perspective, this page examines the Paraspeckle's function through NEAT1, NONO (p45nrb) and SFPQ (PSF).

One aspect of the Molecular function is the Paraspeckle's ability to sequester other molecules affecting transcription. This is done by both NEAT1 and some constituent proteins. NEAT1 is primarily responsible for the Paraspeckle's architecture and providing stability to the protein components.^[11] Yet, it has also been shown to regulate gene expression. This is done by recruitingtranscription factors, sequestering them fromgene promoters and ultimately altering transcription.^[5][16][17] Furthermore, Wang, Z, Li K, Huang, W (2019)^[11] state that NEAT1 can regulate expression by associating withRNA-binding proteins this regulatesRNA splicing events and can manipulate the stability of proteins. Another form of molecule sequestering is through NONO and SFPQ, both proteins can bind to double-stranded RNA that has formed as a result of transcribed inverted repeat motifs.^[9]

Another aspect of molecular function is NEAT1's localisation of Paraspeckle proteins to direct their activity. In a study by Hirose, T. et al. (2014),^[6] when NEAT1_2 levels increase, Paraspeckles elongate. This, in turn, not only increases Paraspeckle length but also the demand for more Paraspeckle proteins to build the tertiary structures required for proper functioning. This reducesnucleoplasmic protein availability. It was noted in their study that this has an impact on the role of free Paraspeckle proteins such asSFPQ which normally represses IL-8, an immune-responsive gene, or can activate theADARB2 gene. Thus, gene regulation can be manipulated not just through sequestering of non-constituent proteins but also Paraspeckle constitutive proteins.

• TheNuclear Compartments:Paraspeckle page on the Nuclear Protein Database, written by Dr. Archa Fox and Dr. Wendy Bickmore, provides a factsheet and links to information on paraspeckle components.

• Cell anatomy
• Organelles
• Nuclear substructures
• Cell nucleus

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• Short description matches Wikidata