Zoology - Research Publications

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    Placental expression of pituitary hormones is an ancestral feature of therian mammals
    Menzies, BR ; Pask, AJ ; Renfree, MB (BMC, 2011)
    BACKGROUND: The placenta is essential for supplying nutrients and gases to the developing mammalian young before birth. While all mammals have a functional placenta, only in therian mammals (marsupials and eutherians) does the placenta closely appose or invade the uterine endometrium. The eutherian placenta secretes hormones that are structurally and functionally similar to pituitary growth hormone (GH), prolactin (PRL) and luteinizing hormone (LH). Marsupial and eutherian mammals diverged from a common ancestor approximately 125 to 148 million years ago and developed distinct reproductive strategies. As in eutherians, marsupials rely on a short-lived but functional placenta for embryogenesis. RESULTS: We characterized pituitary GH, GH-R, IGF-2, PRL and LHβ in a macropodid marsupial, the tammar wallaby, Macropus eugenii. These genes were expressed in the tammar placenta during the last third of gestation when most fetal growth occurs and active organogenesis is initiated. The mRNA of key growth genes GH, GH-R, IGF-2 and PRL were expressed during late pregnancy. We found significant up-regulation of GH, GH-R and IGF-2 after the start of the rapid growth phase of organogenesis which suggests that the placental growth hormones regulate the rapid phase of fetal growth. CONCLUSIONS: This is the first demonstration of the existence of pituitary hormones in the marsupial placenta. Placental expression of these pituitary hormones has clearly been conserved in marsupials as in eutherian mammals, suggesting an ancestral origin of the evolution of placental expression and a critical function of these hormones in growth and development of all therian mammals.
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    Genome sequence of an Australian kangaroo, Macropus eugenii, provides insight into the evolution of mammalian reproduction and development
    Renfree, MB ; Papenfuss, AT ; Deakin, JE ; Lindsay, J ; Heider, T ; Belov, K ; Rens, W ; Waters, PD ; Pharo, EA ; Shaw, G ; Swwong, E ; Lefevre, CM ; Nicholas, KR ; Kuroki, Y ; Wakefield, MJ ; Zenger, KR ; Wang, C ; Ferguson-Smith, M ; Nicholas, FW ; Hickford, D ; Yu, H ; Short, KR ; Siddle, HV ; Frankenberg, SR ; Chew, KY ; Menzies, BR ; Stringer, JM ; Suzuki, S ; Hore, TA ; Delbridge, ML ; Mohammadi, A ; Schneider, NY ; Hu, Y ; O'Hara, W ; Al Nadaf, S ; Wu, C ; Feng, Z-P ; Cocks, BG ; Wang, J ; Flicek, P ; Searle, SMJ ; Fairley, S ; Beal, K ; Herrero, J ; Carone, DM ; Suzuki, Y ; Sugano, S ; Toyoda, A ; Sakaki, Y ; Kondo, S ; Nishida, Y ; Tatsumoto, S ; Mandiou, I ; Hsu, A ; McColl, KA ; Lansdell, B ; Weinstock, G ; Kuczek, E ; McGrath, A ; Wilson, P ; Men, A ; Hazar-Rethinam, M ; Hall, A ; Davis, J ; Wood, D ; Williams, S ; Sundaravadanam, Y ; Muzny, DM ; Jhangiani, SN ; Lewis, LR ; Morgan, MB ; Okwuonu, GO ; Ruiz, SJ ; Santibanez, J ; Nazareth, L ; Cree, A ; Fowler, G ; Kovar, CL ; Dinh, HH ; Joshi, V ; Jing, C ; Lara, F ; Thornton, R ; Chen, L ; Deng, J ; Liu, Y ; Shen, JY ; Song, X-Z ; Edson, J ; Troon, C ; Thomas, D ; Stephens, A ; Yapa, L ; Levchenko, T ; Gibbs, RA ; Cooper, DW ; Speed, TP ; Fujiyama, A ; Graves, JAM ; O'Neill, RJ ; Pask, AJ ; Forrest, SM ; Worley, KC (BMC, 2011)
    BACKGROUND: We present the genome sequence of the tammar wallaby, Macropus eugenii, which is a member of the kangaroo family and the first representative of the iconic hopping mammals that symbolize Australia to be sequenced. The tammar has many unusual biological characteristics, including the longest period of embryonic diapause of any mammal, extremely synchronized seasonal breeding and prolonged and sophisticated lactation within a well-defined pouch. Like other marsupials, it gives birth to highly altricial young, and has a small number of very large chromosomes, making it a valuable model for genomics, reproduction and development. RESULTS: The genome has been sequenced to 2 × coverage using Sanger sequencing, enhanced with additional next generation sequencing and the integration of extensive physical and linkage maps to build the genome assembly. We also sequenced the tammar transcriptome across many tissues and developmental time points. Our analyses of these data shed light on mammalian reproduction, development and genome evolution: there is innovation in reproductive and lactational genes, rapid evolution of germ cell genes, and incomplete, locus-specific X inactivation. We also observe novel retrotransposons and a highly rearranged major histocompatibility complex, with many class I genes located outside the complex. Novel microRNAs in the tammar HOX clusters uncover new potential mammalian HOX regulatory elements. CONCLUSIONS: Analyses of these resources enhance our understanding of marsupial gene evolution, identify marsupial-specific conserved non-coding elements and critical genes across a range of biological systems, including reproduction, development and immunity, and provide new insight into marsupial and mammalian biology and genome evolution.
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    Ultrasonography of wallaby prenatal development shows that the climb to the pouch begins in utero
    Drews, B ; Roellig, K ; Menzies, BR ; Shaw, G ; Buentjen, I ; Herbert, CA ; Hildebrandt, TB ; Renfree, MB (NATURE PUBLISHING GROUP, 2013-03-15)
    Marsupials have a functional placenta for a shorter period of time compared to that of eutherian species, and their altricial young reach the teats without any help from the mother. We have monitored the short intrauterine development of one marsupial, the tammar wallaby, with high-resolution ultrasound from reactivation of the 100-cell diapausing blastocyst to birth. The expanding blastocyst could be visualized when it had reached a diameter of 1.5 mm. From at least halfway through pregnancy, there are strong undulating movements of the endometrium that massage the expanding vesicle against the highly secretory endometrial surface. These unique movements possibly enhance exchange of uterine secretions and gases between the mother and embryo. There was a constant rate of development measured ultrasonographically from mid-gestation, regardless of when the blastocyst reactivated. Interestingly climbing movements by the fetus began in utero about 3 days before birth, mimicking those required to climb to the pouch.