2011
DOI: 10.1098/rstb.2011.0001
|View full text |Cite
|
Sign up to set email alerts
|

Evo-devo, deep homology and FoxP2: implications for the evolution of speech and language

Abstract: The evolution of novel morphological features, such as feathers, involves the modification of developmental processes regulated by gene networks. The fact that genetic novelty operates within developmental constraints is the central tenet of the 'evo-devo' conceptual framework. It is supported by findings that certain molecular regulatory pathways act in a similar manner in the development of morphological adaptations, which are not directly related by common ancestry but evolved convergently. The Pax6 gene, i… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
113
0

Year Published

2012
2012
2020
2020

Publication Types

Select...
7
2
1

Relationship

1
9

Authors

Journals

citations
Cited by 104 publications
(115 citation statements)
references
References 180 publications
(250 reference statements)
2
113
0
Order By: Relevance
“…Another nice example of deep homology is the importance of FoxP2 in vocal learning in humans and birds (Fitch, 2009b(Fitch, , 2011aScharff & Petri, 2011)-the same gene plays an important role in regulating vocal learning in these clades, but the ability itself was not present in the common ancestor of birds and mammals. Deep homology is important because there is increasing evidence that it is common and relevant in the evolution of cognition (Arendt, 2005;Parker et al, 2013;Salas, Broglio, & Rodríguez, 2003).…”
Section: The Broad Comparative Approachmentioning
confidence: 99%
“…Another nice example of deep homology is the importance of FoxP2 in vocal learning in humans and birds (Fitch, 2009b(Fitch, , 2011aScharff & Petri, 2011)-the same gene plays an important role in regulating vocal learning in these clades, but the ability itself was not present in the common ancestor of birds and mammals. Deep homology is important because there is increasing evidence that it is common and relevant in the evolution of cognition (Arendt, 2005;Parker et al, 2013;Salas, Broglio, & Rodríguez, 2003).…”
Section: The Broad Comparative Approachmentioning
confidence: 99%
“…Similarly to children acquiring spoken language, juvenile zebra finches learn their vocalizations incrementally during a critical period by imitating an adult (Bolhuis et al 2010). The neural circuitry underlying vocal learning appears to be partly shared by humans and songbirds, despite these species being separated by large evolutionary distances, pointing to a deep homology (Fisher and Scharff 2009;Scharff and Petri 2011). Furthermore, the zebra finch genome has been sequenced, and sophisticated genetic experiments are possible in this species, such as the identification of neural molecules regulated by vocal behavior (Hilliard et al 2012), and the manipulation of the expression levels of genes of interest during the critical song-learning period (Haesler et al 2007).…”
Section: Insights From Animal Communicationmentioning
confidence: 99%
“…As with the mouse models, neural plasticity in striatal circuitry emerges as a common theme associated with this gene (Murugan et al, 2013;Schulz et al, 2010). There is insufficient space available in this chapter to give a full account of all the relevant songbird studies; for further information on this burgeoning area of work, the interested reader is referred to reviews by Bolhuis et al (2010), Petri (2011), andWohlgemuth et al (2014).…”
Section: Insights From Animal Modelsmentioning
confidence: 99%