Evidence map›Paper›PMID 33030403›Full record

ReviewNucleus (Austin, Tex.)2020

Nuclear lamin phosphorylation: an emerging role in gene regulation and pathogenesis of laminopathies.

Sunny Yang Liu, Kohta Ikegami

Open access · goldAbstract readReviewVideo-Audio Media
In one paragraph

Review in Nucleus (Austin, Tex.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.2field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 75 citations in OpenAlex.

  1. A highly penetrantbioRxiv : the preprint server for biology · 2026
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  7. Co-morbid monogenic disorders at chromosome region 1q2: LMNA- and FLG-related disorders in a patient referred for assessment of joint hypermobility.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 1 country.

Sunny Yang LiuDepartment of Pediatrics, The University of Chicago , Chicago, Illinois, USA.
Kohta IkegamiDepartment of Pediatrics, The University of Chicago , Chicago, Illinois, USA.ORCID 0000-0002-0405-1193
Cincinnati Children's Hospital Medical Center · USUniversity of Chicago · US

Funding

Mechanisms in Lamin A function in gene regulationR33AG054770 · NIA · UNIVERSITY OF CHICAGO · PI IKEGAMI, KOHTA · 2019 to 2021
$1.6M
Mechanisms in Lamin A function in gene regulationR21AG054770 · NIA · UNIVERSITY OF CHICAGO · PI IKEGAMI, KOHTA · 2017 to 2018
$410k
NIA NIH HHS R21 AG054770NIA NIH HHS R33 AG054770
6 · The paper itself

Abstract

Decades of studies have established that nuclear lamin polymers form the nuclear lamina, a protein meshwork that supports the nuclear envelope structure and tethers heterochromatin to the nuclear periphery. Much less is known about unpolymerized nuclear lamins in the nuclear interior, some of which are now known to undergo specific phosphorylation. A recent finding that phosphorylated lamins bind gene enhancer regions offers a new hypothesis that lamin phosphorylation may influence transcriptional regulation in the nuclear interior. In this review, we discuss the regulation, localization, and functions of phosphorylated lamins. We summarize kinases that phosphorylate lamins in a variety of biological contexts. Our discussion extends to laminopathies, a spectrum of degenerative disorders caused by lamin gene mutations, such as cardiomyopathies and progeria. We compare the prevailing hypothesis for laminopathy pathogenesis based on lamins' function at the nuclear lamina with an emerging hypothesis based on phosphorylated lamins' function in the nuclear interior.

Indexed as

AnimalsCardiomyopathy, DilatedHumansLaminsNuclear LaminaPhosphorylationProgeriaLaminscardiomyopathiescdk1chromatinchromosomec-Junenhancerfarnesylationinterphaselamina-associated domainlamin A/Claminopathieslmnamitosismuscular dystrophynuclear interiorNuclear laminphosphorylationprogeria

Identifiers

PMID33030403
PMCPMC7588210
OpenAlexW3092632617

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.