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Keegan, K.

Publications and source records attributed to Keegan, K..

3 recordsLinked to original sources

Has recombination changed during the recent evolution of the guppy Y chromosome?

Genome sequencing and genetic mapping of molecular markers has demonstrated Y-linkage across most of the guppy (Poecilia reticulata) XY chromosome pair. However, they also revealed exchanges with the X, consistent with classical genetic observations of occasional exchanges of factors controlling visible male-specific phenotypic traits. It remains unclear whether this fish species has an extensive sex-determining region without crossing over (whose suppressed recombination could have evolved under selection created by sexually antagonistic effects of male coloration factors), or whether the fully Y-linked region is very small, perhaps within a single gene. Population genomic data support cytogenetic results indicating that it is within the terminal 5 Mb of the 26.5 Mb chromosome 12, just proximal to a highly recombining pseudo-autosomal region, PAR1. Using molecular markers, we studied recombination, focusing on this region of the XY pair. Despite assembly errors in the small terminal PAR1, our mapping identifies very similar genetic PAR boundaries in sires from four populations, suggesting that their crossover patterns have not changed. Our results also confirmed occasional crossovers proximal to the male-determining region, defining a second pseudo-autosomal region, PAR2, recombining much more rarely than PAR1. The crossover positions suggest that the male-determining factor is within a repetitive region near 21 Mb in the female assembly. A sex-reversed XX male had few crossovers in PAR2, suggesting that this regions low crossover rate depends on the phenotypic, not the genetic, sex. Thus rare sex changes, and/or occasional crossovers in males can explain the failure to detect fully Y-linked variants.

genetics↗

Amelioration of Brain Histone Methylopathies by Balancing a Writer-Eraser Duo KMT2A-KDM5C

Histone H3 lysine 4 methylation (H3K4me) is extensively regulated by numerous writer and eraser enzymes in mammals. Nine H3K4me enzymes are associated with neurodevelopmental disorders to date, indicating their important roles in the brain. However, interplay among H3K4me enzymes during brain development remains largely unknown. Here, we show functional interactions of a writer-eraser duo, KMT2A and KDM5C, which are responsible for Wiedemann-Steiner Syndrome (WDSTS), and mental retardation X-linked syndromic Claes-Jensen type (MRXSCJ), respectively. Despite opposite enzymatic activities, the two mouse models deficient for either Kmt2a or Kdm5c shared reduced dendritic spines and increased aggression. Double mutation of Kmt2a and Kdm5c clearly reversed dendritic morphology, key behavioral traits including aggression, and partially corrected altered transcriptomes and H3K4me landscapes. Thus, our study uncovers common yet mutually suppressive aspects of the WDSTS and MRXSCJ models and provides a proof of principle for balancing a single writer-eraser pair to ameliorate their associated disorders.

genetics↗

Disarticulating and Reassembling Amphipyrinae (Lepidoptera, Noctuoidea, Noctuidae)

Amphipyrinae have long been a catchall taxon for Noctuidae, with most members lacking discernible morphological synapomorphies that would allow their assignment to one of the many readily diagnosable noctuid subfamilies. Here data from seven gene regions (>5,500 base pairs) for more than 120 noctuid genera are used to infer a phylogeny for Amphipyrinae and related subfamilies. Sequence data for 57 amphipyrine genera--most represented by the type species of the genus--are examined. Presented here are: the first large-scale molecular phylogenetic study of Amphipyrinae and largest molecular phylogeny of Noctuidae to date; several proposed nomenclatural changes for well supported results; and the identification of areas of noctuid phylogeny where greater taxon sampling and/or genomic-scale data are needed. Adult and larval morphology, along with life history traits, for taxonomic groupings most relevant to the results are discussed. Amphipyrinae are significantly redefined; many former amphipyrines, excluded as a result of these analyses, are reassigned to other noctuid subfamily-level taxa. Four genera, Chamaeclea Grote, Heminocloa Barnes & Benjamin, Hemioslaria Barnes & Benjamin, and Thurberiphaga Dyar are transferred to the tribe Chamaecleini Keegan & Wagner New Tribe in Acontiinae. Stiriina is elevated to Stiriinae Revised Status, Grotellina is elevated to Grotellinae Revised Status, and Annaphilina is elevated to Annaphilini Revised Status. Acopa Harvey is transferred to Bryophilinae, Aleptina Dyar is transferred to Condicinae, Leucocnemis Hampson and Oxycnemis gracillinea (Grote) are transferred to Oncocnemidinae, Nacopa Barnes & Benjamin is transferred to Noctuinae, and Narthecophora Smith is transferred to Stiriinae. Azenia Grote (and its subtribe Azeniina), Cropia Walker, Metaponpneumata Moschler, Sexserrata Barnes & Benjamin, and Tristyla Smith are transferred to Noctuidae incertae sedis. Hemigrotella Barnes & McDunnough (formerly in subtribe Grotellina) is retained in Amphipyrinae.\n\nThis published work has been registered in ZooBank, http://zoobank.org/urn:lsid:zoobank.org:pub:4A140782-31BA-445A-B7BA-6EAB98ED43FA

evolutionary biology↗