Development of a lethal congenital heart defect in the splotch (Pax3) mutant mouse

Simon Conway, Deborah J. Henderson, Margaret L. Kirby, Robert H. Anderson, Andrew J. Copp

Research output: Contribution to journalArticle

106 Citations (Scopus)

Abstract

Objective: The splotch (Sp(2H)) mutation disrupts the Pax3 gene and is lethal in homozygotes. The aim of the present study was to investigate the cause of lethality. Methods and results: Using the splotch (Sp(2H)) mouse mutant, we demonstrated that approximately 60% of Sp(2H) homozygotes die in utero at 13.5-14.5 days of gestation. All these embryos have cardiac malformations involving partial or complete failure of septation of the outflow tract. Although the cause of death in utero is unknown, the dying embryos are edematous, their superior caval veins are over-expanded, and the fetal liver is enlarged and engorged with blood, all signs of cardiac failure. The remaining Sp(2H) homozygotes die around the time of birth, and these embryos have grossly normal hearts. All Sp(2H) homozygotes have neural tube defects, ether spina bifida, exencephaly, or both. Although these defects clearly do not cause death in utero, they are very likely responsible for the perinatal death of homozygotes that survive to late gestation. There is no correlation between the presence or absence of a cardiac defect and the type of neural tube defect. On the other hand, there is a striking correlation between presence of a cardiac defect and reduction or absence of dorsal root ganglia which are derivatives of the neural crest. Conclusions: In this paper, we show that the lethality has a biphasic pattern, and the data strongly suggests that mid-gestation lethality is due to cardiac defects and not the associated neural tube defects. This finding supports the idea that 'conotruncal' cardiac defects involving the ventricular outflow tracts develop as a result of failure of the 'cardiac' neural crest to colonise the developing heart in the mid-gestation embryo, and that the resulting heart defects are solely responsible for the observed mortality.

Original languageEnglish (US)
Pages (from-to)163-173
Number of pages11
JournalCardiovascular Research
Volume36
Issue number2
DOIs
StatePublished - Nov 1997
Externally publishedYes

Fingerprint

Congenital Heart Defects
Homozygote
Neural Tube Defects
Embryonic Structures
Pregnancy
Neural Crest
Cause of Death
Heart Failure
Lethal Genes
Venae Cavae
Spinal Dysraphism
Hepatomegaly
Spinal Ganglia
Ether
Veins
Parturition
Mutation
Mortality

Keywords

  • Cardiac neural crest
  • Congenital heart disease
  • Heart failure
  • Mouse mutant
  • Neural tube defects
  • Pax
  • Splotch

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

Cite this

Development of a lethal congenital heart defect in the splotch (Pax3) mutant mouse. / Conway, Simon; Henderson, Deborah J.; Kirby, Margaret L.; Anderson, Robert H.; Copp, Andrew J.

In: Cardiovascular Research, Vol. 36, No. 2, 11.1997, p. 163-173.

Research output: Contribution to journalArticle

Conway, Simon ; Henderson, Deborah J. ; Kirby, Margaret L. ; Anderson, Robert H. ; Copp, Andrew J. / Development of a lethal congenital heart defect in the splotch (Pax3) mutant mouse. In: Cardiovascular Research. 1997 ; Vol. 36, No. 2. pp. 163-173.
@article{93caf7909a2944ccbdbb6e36475cd7e4,
title = "Development of a lethal congenital heart defect in the splotch (Pax3) mutant mouse",
abstract = "Objective: The splotch (Sp(2H)) mutation disrupts the Pax3 gene and is lethal in homozygotes. The aim of the present study was to investigate the cause of lethality. Methods and results: Using the splotch (Sp(2H)) mouse mutant, we demonstrated that approximately 60{\%} of Sp(2H) homozygotes die in utero at 13.5-14.5 days of gestation. All these embryos have cardiac malformations involving partial or complete failure of septation of the outflow tract. Although the cause of death in utero is unknown, the dying embryos are edematous, their superior caval veins are over-expanded, and the fetal liver is enlarged and engorged with blood, all signs of cardiac failure. The remaining Sp(2H) homozygotes die around the time of birth, and these embryos have grossly normal hearts. All Sp(2H) homozygotes have neural tube defects, ether spina bifida, exencephaly, or both. Although these defects clearly do not cause death in utero, they are very likely responsible for the perinatal death of homozygotes that survive to late gestation. There is no correlation between the presence or absence of a cardiac defect and the type of neural tube defect. On the other hand, there is a striking correlation between presence of a cardiac defect and reduction or absence of dorsal root ganglia which are derivatives of the neural crest. Conclusions: In this paper, we show that the lethality has a biphasic pattern, and the data strongly suggests that mid-gestation lethality is due to cardiac defects and not the associated neural tube defects. This finding supports the idea that 'conotruncal' cardiac defects involving the ventricular outflow tracts develop as a result of failure of the 'cardiac' neural crest to colonise the developing heart in the mid-gestation embryo, and that the resulting heart defects are solely responsible for the observed mortality.",
keywords = "Cardiac neural crest, Congenital heart disease, Heart failure, Mouse mutant, Neural tube defects, Pax, Splotch",
author = "Simon Conway and Henderson, {Deborah J.} and Kirby, {Margaret L.} and Anderson, {Robert H.} and Copp, {Andrew J.}",
year = "1997",
month = "11",
doi = "10.1016/S0008-6363(97)00172-7",
language = "English (US)",
volume = "36",
pages = "163--173",
journal = "Cardiovascular Research",
issn = "0008-6363",
publisher = "Oxford University Press",
number = "2",

}

TY - JOUR

T1 - Development of a lethal congenital heart defect in the splotch (Pax3) mutant mouse

AU - Conway, Simon

AU - Henderson, Deborah J.

AU - Kirby, Margaret L.

AU - Anderson, Robert H.

AU - Copp, Andrew J.

PY - 1997/11

Y1 - 1997/11

N2 - Objective: The splotch (Sp(2H)) mutation disrupts the Pax3 gene and is lethal in homozygotes. The aim of the present study was to investigate the cause of lethality. Methods and results: Using the splotch (Sp(2H)) mouse mutant, we demonstrated that approximately 60% of Sp(2H) homozygotes die in utero at 13.5-14.5 days of gestation. All these embryos have cardiac malformations involving partial or complete failure of septation of the outflow tract. Although the cause of death in utero is unknown, the dying embryos are edematous, their superior caval veins are over-expanded, and the fetal liver is enlarged and engorged with blood, all signs of cardiac failure. The remaining Sp(2H) homozygotes die around the time of birth, and these embryos have grossly normal hearts. All Sp(2H) homozygotes have neural tube defects, ether spina bifida, exencephaly, or both. Although these defects clearly do not cause death in utero, they are very likely responsible for the perinatal death of homozygotes that survive to late gestation. There is no correlation between the presence or absence of a cardiac defect and the type of neural tube defect. On the other hand, there is a striking correlation between presence of a cardiac defect and reduction or absence of dorsal root ganglia which are derivatives of the neural crest. Conclusions: In this paper, we show that the lethality has a biphasic pattern, and the data strongly suggests that mid-gestation lethality is due to cardiac defects and not the associated neural tube defects. This finding supports the idea that 'conotruncal' cardiac defects involving the ventricular outflow tracts develop as a result of failure of the 'cardiac' neural crest to colonise the developing heart in the mid-gestation embryo, and that the resulting heart defects are solely responsible for the observed mortality.

AB - Objective: The splotch (Sp(2H)) mutation disrupts the Pax3 gene and is lethal in homozygotes. The aim of the present study was to investigate the cause of lethality. Methods and results: Using the splotch (Sp(2H)) mouse mutant, we demonstrated that approximately 60% of Sp(2H) homozygotes die in utero at 13.5-14.5 days of gestation. All these embryos have cardiac malformations involving partial or complete failure of septation of the outflow tract. Although the cause of death in utero is unknown, the dying embryos are edematous, their superior caval veins are over-expanded, and the fetal liver is enlarged and engorged with blood, all signs of cardiac failure. The remaining Sp(2H) homozygotes die around the time of birth, and these embryos have grossly normal hearts. All Sp(2H) homozygotes have neural tube defects, ether spina bifida, exencephaly, or both. Although these defects clearly do not cause death in utero, they are very likely responsible for the perinatal death of homozygotes that survive to late gestation. There is no correlation between the presence or absence of a cardiac defect and the type of neural tube defect. On the other hand, there is a striking correlation between presence of a cardiac defect and reduction or absence of dorsal root ganglia which are derivatives of the neural crest. Conclusions: In this paper, we show that the lethality has a biphasic pattern, and the data strongly suggests that mid-gestation lethality is due to cardiac defects and not the associated neural tube defects. This finding supports the idea that 'conotruncal' cardiac defects involving the ventricular outflow tracts develop as a result of failure of the 'cardiac' neural crest to colonise the developing heart in the mid-gestation embryo, and that the resulting heart defects are solely responsible for the observed mortality.

KW - Cardiac neural crest

KW - Congenital heart disease

KW - Heart failure

KW - Mouse mutant

KW - Neural tube defects

KW - Pax

KW - Splotch

UR - http://www.scopus.com/inward/record.url?scp=0031281314&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0031281314&partnerID=8YFLogxK

U2 - 10.1016/S0008-6363(97)00172-7

DO - 10.1016/S0008-6363(97)00172-7

M3 - Article

VL - 36

SP - 163

EP - 173

JO - Cardiovascular Research

JF - Cardiovascular Research

SN - 0008-6363

IS - 2

ER -