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Skeletal element elongation and interdigital tissue regression in developing bat limbs: a gene expression analysis

Vertebrate limbs classically illustrate the morphological diversity of homologous structure. Bat limbs exemplify this, having strikingly divergent limbs: wings with asymmetrically elongated digit elements, supporting expansive membranes; and hindlimbs with short, symmetrical, free digits. An under...

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Main Author: Mason, Mandy K
Other Authors: Illing, Nicola
Format: Thesis
Language:English
Published: Department of Molecular and Cell Biology 2016
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access_status_str Open Access
author Mason, Mandy K
author2 Illing, Nicola
author_browse Illing, Nicola
Mason, Mandy K
author_facet Illing, Nicola
Mason, Mandy K
author_sort Mason, Mandy K
collection Thesis
description Vertebrate limbs classically illustrate the morphological diversity of homologous structure. Bat limbs exemplify this, having strikingly divergent limbs: wings with asymmetrically elongated digit elements, supporting expansive membranes; and hindlimbs with short, symmetrical, free digits. An understanding of the genes, interactions and events that shape bat limbs, will inform conventional models of development. This dissertation characterised differential expression of Meis2, in the context of interdigital regression, and the 5'HoxD genes in the context of digit formation in developing bat autopods (CS15 - CS18). Meis2 is involved in limb proximodistal patterning, and has been shown to promote proliferation, and survival of cells in other developmental contexts. Meis2 had strong expression in the expanding bat forelimb interdigits, with lowered expression in mouse and bat hindlimb interdigits, and did not correspond with Hoxa13 expression, which was reduced in the forelimb. Autopod expression was independent of retinoic acid (RA) signalling, with genes involved in RA synthesis ( Rdh10 , Aldha2 ) , degradation ( Cyp26b1 ) and signalling (Rar β) expressed in bat limbs. Altered expression patterns of Aldha2 and Cyp26b1, indicate that this pathway may be modulated in the forelimb. Meis2 is suggested to play a role in interdigital tissue retention, enhancing cell proliferation and contributing to wing expansion. 5'HoxD genes (Hoxd10 - 13) are involved in limb patterning, digit formation and growth. Their modular autopod expression domains correspond to the bat skeletal element phenotype, with strong overexpression of Hoxd10 - 11 (and to a lesser extent Hoxd12) in the forelimb posterior elements (digits II - V), which are highly elongated, and a loss of expression of these genes in hindlimb digits. These genes were not expressed in a typical reverse collinear relationship, with absolute q PCR revealing highest expression of Hoxd10. While the coding protein sequence of these genes appeared highly conserved between bats and other mammals, several changes were found in the CsC region of the digit enhancer Prox, some of which were associated with alterations in transcription binding sites. These findings indicate that Hoxd10 - 12 expressions contribute to the altered skeletal element morphologies of bat forelimbs and hindlimbs. This study makes a valuable contribution to the growing body of work that explores bat limb development and the evolutionary adaptation s of these unique structures.
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institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:34:38.153Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2016
publishDateRange 2016
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publisher Department of Molecular and Cell Biology
publisherStr Department of Molecular and Cell Biology
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source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/20293 Skeletal element elongation and interdigital tissue regression in developing bat limbs: a gene expression analysis Mason, Mandy K Illing, Nicola Jacobs, David S Molecular and Cell Biology Vertebrate limbs classically illustrate the morphological diversity of homologous structure. Bat limbs exemplify this, having strikingly divergent limbs: wings with asymmetrically elongated digit elements, supporting expansive membranes; and hindlimbs with short, symmetrical, free digits. An understanding of the genes, interactions and events that shape bat limbs, will inform conventional models of development. This dissertation characterised differential expression of Meis2, in the context of interdigital regression, and the 5'HoxD genes in the context of digit formation in developing bat autopods (CS15 - CS18). Meis2 is involved in limb proximodistal patterning, and has been shown to promote proliferation, and survival of cells in other developmental contexts. Meis2 had strong expression in the expanding bat forelimb interdigits, with lowered expression in mouse and bat hindlimb interdigits, and did not correspond with Hoxa13 expression, which was reduced in the forelimb. Autopod expression was independent of retinoic acid (RA) signalling, with genes involved in RA synthesis ( Rdh10 , Aldha2 ) , degradation ( Cyp26b1 ) and signalling (Rar β) expressed in bat limbs. Altered expression patterns of Aldha2 and Cyp26b1, indicate that this pathway may be modulated in the forelimb. Meis2 is suggested to play a role in interdigital tissue retention, enhancing cell proliferation and contributing to wing expansion. 5'HoxD genes (Hoxd10 - 13) are involved in limb patterning, digit formation and growth. Their modular autopod expression domains correspond to the bat skeletal element phenotype, with strong overexpression of Hoxd10 - 11 (and to a lesser extent Hoxd12) in the forelimb posterior elements (digits II - V), which are highly elongated, and a loss of expression of these genes in hindlimb digits. These genes were not expressed in a typical reverse collinear relationship, with absolute q PCR revealing highest expression of Hoxd10. While the coding protein sequence of these genes appeared highly conserved between bats and other mammals, several changes were found in the CsC region of the digit enhancer Prox, some of which were associated with alterations in transcription binding sites. These findings indicate that Hoxd10 - 12 expressions contribute to the altered skeletal element morphologies of bat forelimbs and hindlimbs. This study makes a valuable contribution to the growing body of work that explores bat limb development and the evolutionary adaptation s of these unique structures. 2016-07-11T13:49:52Z 2016-07-11T13:49:52Z 2016 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/20293 eng application/pdf Department of Molecular and Cell Biology Faculty of Science University of Cape Town
spellingShingle Molecular and Cell Biology
Mason, Mandy K
Skeletal element elongation and interdigital tissue regression in developing bat limbs: a gene expression analysis
thesis_degree_str Doctoral
title Skeletal element elongation and interdigital tissue regression in developing bat limbs: a gene expression analysis
title_full Skeletal element elongation and interdigital tissue regression in developing bat limbs: a gene expression analysis
title_fullStr Skeletal element elongation and interdigital tissue regression in developing bat limbs: a gene expression analysis
title_full_unstemmed Skeletal element elongation and interdigital tissue regression in developing bat limbs: a gene expression analysis
title_short Skeletal element elongation and interdigital tissue regression in developing bat limbs: a gene expression analysis
title_sort skeletal element elongation and interdigital tissue regression in developing bat limbs a gene expression analysis
topic Molecular and Cell Biology
url http://hdl.handle.net/11427/20293
work_keys_str_mv AT masonmandyk skeletalelementelongationandinterdigitaltissueregressionindevelopingbatlimbsageneexpressionanalysis