Evidence map›Paper›PMID 25486194›Full record

ArticleCell cycle (Georgetown, Tex.)2014

Replication-dependent histone genes are actively transcribed in differentiating and aging retinal neurons.

Abdul Rouf Banday, Marybeth Baumgartner, Sahar Al Seesi, Devi Krishna Priya Karunakaran, Aditya Venkatesh, Sean Congdon, Christopher Lemoine, Ashley M Kilcollins, Ion Mandoiu, Claudio Punzo and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

18 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  4. GlialProceedings of the National Academy of Sciences of the United States of America · 2024
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  7. Sample multiplexing for targeted pathway proteomics in aging mice.Proceedings of the National Academy of Sciences of the United States of America · 2020
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  18. Observational
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

11 authors at 1 institution in 1 country.

Abdul Rouf Bandaya Department of Physiology and Neurobiology ; University of Connecticut ; Storrs , CT USA.
Marybeth Baumgartner
Sahar Al Seesi
Devi Krishna Priya Karunakaran
Aditya Venkatesh
Sean Congdon
Christopher Lemoine
Ashley M Kilcollins
Ion Mandoiu
Claudio Punzo
Rahul N Kanadia
Massachusetts Academy of Math and Science at WPI · US

Funding

Recruitment of Neurobiology Faculty at the University of ConnecticutP30NS069266 · NINDS · UNIVERSITY OF CONNECTICUT STORRS · PI RENFRO, JAMES LARRY · 2009 to 2010
$1.3M
The Role of Alternative Splicing Factor Sfrs10 in Neural DevelopmentR00EY019547 · NEI · UNIVERSITY OF CONNECTICUT STORRS · PI KANADIA, RAHUL N · 2011 to 2013
$569k
NEI NIH HHS 4R00EY019547NEI NIH HHS R00 EY019547NINDS NIH HHS 5P30NS069266NINDS NIH HHS P30 NS069266PHS HHS K99-R00
6 · The paper itself

Abstract

In the mammalian genome, each histone family contains multiple replication-dependent paralogs, which are found in clusters where their transcription is thought to be coupled to the cell cycle. Here, we wanted to interrogate the transcriptional regulation of these paralogs during retinal development and aging. We employed deep sequencing, quantitative PCR, in situ hybridization (ISH), and microarray analysis, which revealed that replication-dependent histone genes were not only transcribed in progenitor cells but also in differentiating neurons. Specifically, by ISH analysis we found that different histone genes were actively transcribed in a subset of neurons between postnatal day 7 and 14. Interestingly, within a histone family, not all paralogs were transcribed at the same level during retinal development. For example, expression of Hist1h1b was higher embryonically, while that of Hist1h1c was higher postnatally. Finally, expression of replication-dependent histone genes was also observed in the aging retina. Moreover, transcription of replication-dependent histones was independent of rapamycin-mediated mTOR pathway inactivation. Overall, our data suggest the existence of variant nucleosomes produced by the differential expression of the replication-dependent histone genes across retinal development. Also, the expression of a subset of replication-dependent histone isotypes in senescent neurons warrants re-examining these genes as "replication-dependent." Thus, our findings underscore the importance of understanding the transcriptional regulation of replication-dependent histone genes in the maintenance and functioning of neurons.

Indexed as

Transcription, GeneticAnimalsCellular SenescenceCyclin D1Cyclin EDNA ReplicationHistonesMiceNeurogenesisProtein IsoformsRetinal NeuronsRNA, MessengerStem CellsTOR Serine-Threonine KinasesCyclin D1Cyclin EHistonesmTOR protein, mouseProtein IsoformsRNA, MessengerTOR Serine-Threonine KinasesAAamino acidCEChrchromosomecytoplasmic extractdevelopmentexpressionganglion cell layerGCLhistonesINLinner nuclear layerin situ hybridizationISHisotypesNEnuclear extractONBLONLouter neuroblastic layerouter nuclear layerPCRpolymerase chain reactionqPCRquantitative PCRreplication-dependentretinaretinal pigment epitheliumRPEtranscriptionvariant nucleosome

Identifiers

PMID25486194
PMCPMC4614993
OpenAlexW2013324940

What OpenQuestion holds

Textmetadata
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.