Katie Fowler

Dr. Katie Fowler


Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2016 in Theriogenology
Verified
Journal Article
Closed access
AMA.A. Mandawala
A.A. Mandawala
SHS.C. Harvey
S.C. Harvey
TRT.K. Roy
T.K. Roy
KFKatie Fowler
Katie Fowler

11 December 2014 in BMC Genomics
Verified
Journal Article
Open access
PDF file
Michael N. RomanovMichael N. Romanov
Michael N. Romanov
Marta FarréMarta Farré
Marta Farré
PLPamela E Lithgow
Pamela E Lithgow
KFKatie Fowler
Katie Fowler
BSBen Skinner
Ben Skinner
Darren GriffinDarren Griffin
Darren Griffin
The availability of multiple avian genome sequence assemblies greatly improves our ability to define overall genome organization and reconstruct evolutionary changes. In birds, this has previously been impeded by a near intractable karyotype and relied almost exclusively on comparative molecular cytogenetics of only the largest chromosomes. Here, novel whole genome sequence information from 21 avian genome sequences (most newly assembled) made available on an interactive browser (Evolution Highway) was analyzed. Focusing on the six best-assembled genomes allowed us to assemble a putative karyotype of the dinosaur ancestor for each chromosome. Reconstructing evolutionary events that led to each species’ genome organization, we determined that the fastest rate of change occurred in the zebra finch and budgerigar, consistent with rapid speciation events in the Passeriformes and Psittaciformes. Intra- and interchromosomal changes were explained most parsimoniously by a series of inversions and translocations respectively, with breakpoint reuse being commonplace. Analyzing chicken and zebra finch, we found little evidence to support the hypothesis of an association of evolutionary breakpoint regions with recombination hotspots but some evidence to support the hypothesis that microchromosomes largely represent conserved blocks of synteny in the majority of the 21 species analyzed. All but one species showed the expected number of microchromosomal rearrangements predicted by the haploid chromosome count. Ostrich, however, appeared to retain an overall karyotype structure of 2n = 80 despite undergoing a large number (26) of hitherto un-described interchromosomal changes. Results suggest that mechanisms exist to preserve a static overall avian karyotype/genomic structure, including the microchromosomes, with widespread interchromosomal change occurring rarely (e.g., in ostrich and budgerigar lineages). Of the species analyzed, the chicken lineage appeared to have undergone the fewest changes compared to the dinosaur ancestor.

1 September 2018 in Reproductive Biology
Verified
Journal Article
Closed access
KFKatie Fowler
Katie Fowler
AMAnjali A. Mandawala
Anjali A. Mandawala
DGDarren K. Griffin
Darren K. Griffin
GWGrant A. Walling
Grant A. Walling
SHSimon C. Harvey
Simon C. Harvey

1 November 2016 in Animal Reproduction Science
Verified
Journal Article
Closed access
AMA.A. Mandawala
A.A. Mandawala
SHS.C. Harvey
S.C. Harvey
TRT.K. Roy
T.K. Roy
KFKatie Fowler
Katie Fowler

8 May 2018 in Journal of Animal Physiology and Animal Nutrition
Verified
Journal Article
Closed access
PDF file
ESE. G. Smith
E. G. Smith
KDK. Davis
K. Davis
LSL. Sulsh
L. Sulsh
SHS. C. Harvey
S. C. Harvey
KFKatie Fowler
Katie Fowler