Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution (Q21092496)

1

Layla

Parker-Katiraee

1 reference

15 August 2022

Andrew R Carson

2

Andrew R

Carson

1 reference

15 August 2022

Takahiro Yamada

3

Takahiro

Yamada

1 reference

15 August 2022

Sayeda N Abu-Amero

6

Sayeda N

Abu-Amero

1 reference

15 August 2022

Gudrun E Moore

7

Gudrun E

Moore

1 reference

15 August 2022

George H Perry

9

George H

Perry

1 reference

15 August 2022

Charles Lee

11

Charles

Lee

1 reference

15 August 2022

Makiko Meguro-Horike

12

Makiko

Meguro-Horike

1 reference

15 August 2022

Hiroyuki Sasaki

13

Hiroyuki

Sasaki

1 reference

15 August 2022

Keiko Kobayashi

14

Keiko

Kobayashi

1 reference

15 August 2022

Kazuhiko Nakabayashi

15

Kazuhiko

Creative Commons Attribution 4.0 International

Nakabayashi

1 reference

15 August 2022

language of work or name

English

0 references

publication date

4 May 2007

0 references

published in

PLOS Genetics

0 references

volume

3

0 references

page(s)

e65

0 references

issue

5

0 references

copyright license

start time

4 May 2007

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Deficiency of Rbbp1/Arid4a and Rbbp1l1/Arid4b alters epigenetic modifications and suppresses an imprinting defect in the PWS/AS domain

19 March 2017

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Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting

19 March 2017

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Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32

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Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region

19 March 2017

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Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome

19 March 2017

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A forkhead-domain gene is mutated in a severe speech and language disorder

19 March 2017

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A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21

19 March 2017

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19 March 2017

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The novel gene, gamma2-COP (COPG2), in the 7q32 imprinted domain escapes genomic imprinting

19 March 2017

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Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesis

19 March 2017

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19 March 2017

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Evidence against a major role of PEG1/MEST in Silver-Russell syndrome

19 March 2017

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19 March 2017

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19 March 2017

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7 April 2017

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Statistical tests of neutrality of mutations against population growth, hitchhiking and background selection

7 April 2017

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7 April 2017

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Accelerated evolution of nervous system genes in the origin of Homo sapiens

7 April 2017

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Heterochromatin and epigenetic control of gene expression

7 April 2017

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ASPM is a major determinant of cerebral cortical size

7 April 2017

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7 April 2017

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Human LINE retrotransposons generate processed pseudogenes

7 April 2017

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Differential histone modifications mark mouse imprinting control regions during spermatogenesis.

7 April 2017

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Positive selection, relaxation, and acceleration in the evolution of the human and chimp genome

12 September 2017

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Human KLF17 is a new member of the Sp/KLF family of transcription factors

12 September 2017

1 reference

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Weak selection revealed by the whole-genome comparison of the X chromosome and autosomes of human and chimpanzee

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.

12 September 2017

1 reference

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The profile of repeat-associated histone lysine methylation states in the mouse epigenome

12 September 2017

1 reference

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Genomic imprinting of IGF2, p57(KIP2) and PEG1/MEST in a marsupial, the tammar wallaby

12 September 2017

1 reference

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Imprinting along the Kcnq1 domain on mouse chromosome 7 involves repressive histone methylation and recruitment of Polycomb group complexes.

12 September 2017

1 reference

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Pattern of sequence variation across 213 environmental response genes

12 September 2017

1 reference

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Site-specific analysis of histone methylation and acetylation

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome

12 September 2017

1 reference

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Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populations

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

Imprinting analysis of 10 genes and/or transcripts in a 1.5-Mb MEST-flanking region at human chromosome 7q32.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

The potential role of gene duplications in the evolution of imprinting mechanisms

12 September 2017

1 reference

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Insulator and silencer sequences in the imprinted region of human chromosome 11p15.5.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

The Sp1-like protein BTEB3 inhibits transcription via the basic transcription element box by interacting with mSin3A and HDAC-1 co-repressors and competing with Sp1.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

The biology of the mammalian Krüppel-like family of transcription factors

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

Identification of a methylation imprint mark within the mouse Gnas locus

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

Zac1 (Lot1), a potential tumor suppressor gene, and the gene for epsilon-sarcoglycan are maternally imprinted genes: identification by a subtractive screen of novel uniparental fibroblast lines

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

Positive darwinian selection observed at the variable-region genes of immunoglobulins

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

Molecular evolution of an imprinted gene: repeatability of patterns of evolution within the mammalian insulin-like growth factor type II receptor

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

Human-specific amino acid changes found in 103 protein-coding genes.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

The histone code regulating expression of the imprinted mouse Igf2r gene

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

Differential patterns of histone methylation and acetylation distinguish active and repressed alleles at X-linked genes.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

The gene TSGA14, adjacent to the imprinted gene MEST, escapes genomic imprinting.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

Delta-like and gtl2 are reciprocally expressed, differentially methylated linked imprinted genes on mouse chromosome 12.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

Molecular evolution of imprinted genes: no evidence for antagonistic coevolution.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1865561

Variation is the spice of life

29 November 2018

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https://pubmed.ncbi.nlm.nih.gov/17480121