Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease


Autoria(s): Smemo, Scott; Campos, Luciene C.; Moskowitz, Ivan P.; Krieger, Jose E.; Pereira, Alexandre C.; Nobrega, Marcelo A.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

26/08/2013

26/08/2013

2012

Resumo

Recent studies have identified the genetic underpinnings of a growing number of diseases through targeted exome sequencing. However, this strategy ignores the large component of the genome that does not code for proteins, but is nonetheless biologically functional. To address the possible involvement of regulatory variation in congenital heart diseases (CHDs), we searched for regulatory mutations impacting the activity of TBX5, a dosage-dependent transcription factor with well-defined roles in the heart and limb development that has been associated with the HoltOram syndrome (hearthand syndrome), a condition that affects 1/100 000 newborns. Using a combination of genomics, bioinformatics and mouse genetic engineering, we scanned approximate to 700 kb of the TBX5 locus in search of cis-regulatory elements. We uncovered three enhancers that collectively recapitulate the endogenous expression pattern of TBX5 in the developing heart. We re-sequenced these enhancer elements in a cohort of non-syndromic patients with isolated atrial and/or ventricular septal defects, the predominant cardiac defects of the HoltOram syndrome, and identified a patient with a homozygous mutation in an enhancer approximate to 90 kb downstream of TBX5. Notably, we demonstrate that this single-base-pair mutation abrogates the ability of the enhancer to drive expression within the heart in vivo using both mouse and zebrafish transgenic models. Given the population-wide frequency of this variant, we estimate that 1/100 000 individuals would be homozygous for this variant, highlighting that a significant number of CHD associated with TBX5 dysfunction might arise from non-coding mutations in TBX5 heart enhancers, effectively decoupling the heart and hand phenotypes of the HoltOram syndrome.

National Institutes of Health [HL088393, HG004428, DK078871]

National Institutes of Health

Genetics and Regulation Training Grant [T32GM007197]

Genetics and Regulation Training Grant

Identificador

HUMAN MOLECULAR GENETICS, OXFORD, v. 21, n. 14, supl. 1, Part 1, pp. 3255-3263, 42186, 2012

0964-6906

http://www.producao.usp.br/handle/BDPI/32707

10.1093/hmg/dds165

http://dx.doi.org/10.1093/hmg/dds165

Idioma(s)

eng

Publicador

OXFORD UNIV PRESS

OXFORD

Relação

HUMAN MOLECULAR GENETICS

Direitos

closedAccess

Copyright OXFORD UNIV PRESS

Palavras-Chave #HOLT-ORAM-SYNDROME #TRANSCRIPTION FACTORS #COMMON VARIANTS #BINDING SITES #QRS DURATION #CANCER RISK #PR INTERVAL #EXPRESSION #MUTATIONS #ZEBRAFISH #BIOCHEMISTRY & MOLECULAR BIOLOGY #GENETICS & HEREDITY
Tipo

article

original article

publishedVersion