Evidence map›Paper›PMID 34842137›Full record

ArticleeLife2021

Altered temporal sequence of transcriptional regulators in the generation of human cerebellar granule cells.

Hourinaz Behesti, Arif Kocabas, David E Buchholz, Thomas S Carroll, Mary E Hatten

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 28 citations in OpenAlex.

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  5. Histone bivalency in CNS development.Genes & development · 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

5 authors at 1 institution in 1 country.

Hourinaz BehestiLaboratory of Developmental Neurobiology, Rockefeller University, New York, United States.ORCID 0000-0001-9383-9929
Arif KocabasLaboratory of Developmental Neurobiology, Rockefeller University, New York, United States.
David E BuchholzLaboratory of Developmental Neurobiology, Rockefeller University, New York, United States.ORCID 0000-0003-4021-7696
Thomas S CarrollBioinformatics Resource Center, Rockefeller University, New York, United States.
Mary E HattenLaboratory of Developmental Neurobiology, Rockefeller University, New York, United States.ORCID 0000-0001-9059-660X
Rockefeller University · US

Funding

Development of a model system to study human cerebellar neuronsR21NS093540 · NINDS · ROCKEFELLER UNIVERSITY · PI HATTEN, MARY ELIZABETH · 2015 to 2016
$466k
Molecular Mechanisms of Purkinje Cell Degeneration in Ataxia-TelangiectasiaR21NS121438 · NINDS · ROCKEFELLER UNIVERSITY · PI HATTEN, MARY ELIZABETH · 2021 to 2021
$466k
NINDS NIH HHS R21 NS093540NINDS NIH HHS R21 NS121438
6 · The paper itself

Abstract

Brain development is regulated by conserved transcriptional programs across species, but little is known about the divergent mechanisms that create species-specific characteristics. Among brain regions, human cerebellar histogenesis differs in complexity compared with nonhuman primates and rodents, making it important to develop methods to generate human cerebellar neurons that closely resemble those in the developing human cerebellum. We report a rapid protocol for the derivation of the human ATOH1 lineage, the precursor of excitatory cerebellar neurons, from human pluripotent stem cells (hPSCs). Upon transplantation into juvenile mice, hPSC-derived cerebellar granule cells migrated along glial fibers and integrated into the cerebellar cortex. By Translational Ribosome Affinity Purification-seq, we identified an unexpected temporal shift in the expression of RBFOX3 (NeuN) and NEUROD1, which are classically associated with differentiated neurons, in the human outer external granule layer. This molecular divergence may enable the protracted development of the human cerebellum compared to mice.

Indexed as

AnimalsAntigens, NuclearBasic Helix-Loop-Helix ProteinsCell LineCerebellumHumansMiceMice, Inbred C57BLMutationNerve Tissue ProteinsAntigens, NuclearBasic Helix-Loop-Helix ProteinsNerve Tissue ProteinsNEUROD1 protein, humanneuronal nuclear antigen NeuN, humancerebellar granule cellsdevelopmental biologydevelopmental timinghumanhuman cerebellumhuman pluripotent stem cellsmolecular profilingmousequiescent cellsregenerative medicinestem cells

Identifiers

PMID34842137
PMCPMC8687658
OpenAlexW3216123341

What OpenQuestion holds

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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.