Evidence map›Paper›PMID 35978051›Full record

ArticleChromosoma2022

Genome characterization and CRISPR-Cas9 editing of a human neocentromere.

Antonio Palazzo, Ilaria Piccolo, Crescenzio Francesco Minervini, Stefania Purgato, Oronzo Capozzi, Pietro D'Addabbo, Cosimo Cumbo, Francesco Albano, Mariano Rocchi, Claudia Rita Catacchio

Open access · hybridAbstract read
In one paragraph

Article in Chromosoma, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 33% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

10 authors at 2 institutions in 1 country.

Antonio PalazzoDepartment of Biology, University of Bari Aldo Moro, Bari, Italy. antonio.palazzo@uniba.it.
Ilaria PiccoloDepartment of Biology, University of Bari Aldo Moro, Bari, Italy.
Crescenzio Francesco MinerviniDepartment of Emergency and Organ Transplantation (D.E.T.O.), Hematology and Stem Cell Transplantation Unit, University of Bari Aldo Moro, Bari, Italy.
Stefania PurgatoDepartment of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.
Oronzo CapozziDepartment of Biology, University of Bari Aldo Moro, Bari, Italy.
Pietro D'AddabboDepartment of Biology, University of Bari Aldo Moro, Bari, Italy.
Cosimo CumboDepartment of Emergency and Organ Transplantation (D.E.T.O.), Hematology and Stem Cell Transplantation Unit, University of Bari Aldo Moro, Bari, Italy.
Francesco AlbanoDepartment of Emergency and Organ Transplantation (D.E.T.O.), Hematology and Stem Cell Transplantation Unit, University of Bari Aldo Moro, Bari, Italy.
Mariano RocchiDepartment of Biology, University of Bari Aldo Moro, Bari, Italy.
Claudia Rita CatacchioDepartment of Biology, University of Bari Aldo Moro, Bari, Italy. claudiarita.catacchio@uniba.it.
University of Bari Aldo Moro · ITUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The maintenance of genome integrity is ensured by proper chromosome inheritance during mitotic and meiotic cell divisions. The chromosomal counterpart responsible for chromosome segregation to daughter cells is the centromere, at which the spindle apparatus attaches through the kinetochore. Although all mammalian centromeres are primarily composed of megabase-long repetitive sequences, satellite-free human neocentromeres have been described. Neocentromeres and evolutionary new centromeres have revolutionized traditional knowledge about centromeres. Over the past 20 years, insights have been gained into their organization, but in spite of these advancements, the mechanisms underlying their formation and evolution are still unclear. Today, through modern and increasingly accessible genome editing and long-read sequencing techniques, research in this area is undergoing a sudden acceleration. In this article, we describe the primary sequence of a previously described human chromosome 3 neocentromere and observe its possible evolution and repair results after a chromosome breakage induced through CRISPR-Cas9 technologies. Our data represent an exciting advancement in the field of centromere/neocentromere evolution and chromosome stability.

Indexed as

CentromereCRISPR-Cas SystemsAnimalsChromosome BreakageChromosome SegregationHumansKinetochoresMammalsCRISPR-Cas9IsochromosomeLong-read sequencingNeocentromere

Identifiers

PMID35978051
PMCPMC9674717
OpenAlexW4292339994

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.