Using Xenopus to understand human disease and developmental disorders

被引:32
|
作者
Sater, Amy K. [1 ]
Moody, Sally A. [2 ]
机构
[1] Univ Houston, Dept Biol & Biochem, Houston, TX 77004 USA
[2] George Washington Univ, Sch Med & Hlth Sci, Dept Anat & Regenerat Biol, Washington, DC 20052 USA
关键词
Xenopus; embryo; model system; genome; human disease; MODEL ORGANISM DATABASE; LEFT-RIGHT ASYMMETRY; LAEVIS EGG EXTRACTS; OOCYTE 5S DNA; IN-VIVO; NUCLEOTIDE-SEQUENCE; NONCLASSICAL MHC; REPLICATION-FORK; CELL FATE; SCREEN;
D O I
10.1002/dvg.22997
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Model animals are crucial to biomedical research. Among the commonly used model animals, the amphibian, Xenopus, has had tremendous impact because of its unique experimental advantages, cost effectiveness, and close evolutionary relationship with mammals as a tetrapod. Over the past 50years, the use of Xenopus has made possible many fundamental contributions to biomedicine, and it is a cornerstone of research in cell biology, developmental biology, evolutionary biology, immunology, molecular biology, neurobiology, and physiology. The prospects for Xenopus as an experimental system are excellent: Xenopus is uniquely well-suited for many contemporary approaches used to study fundamental biological and disease mechanisms. Moreover, recent advances in high throughput DNA sequencing, genome editing, proteomics, and pharmacological screening are easily applicable in Xenopus, enabling rapid functional genomics and human disease modeling at a systems level.
引用
收藏
页数:14
相关论文
共 50 条
  • [1] Using Developmental Trajectories to Understand Developmental Disorders
    Thomas, Michael S. C.
    Annaz, Dagmara
    Ansari, Daniel
    Scerif, Gaia
    Jarrold, Chris
    Karmiloff-Smith, Annette
    JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH, 2009, 52 (02): : 336 - 358
  • [2] Using neuroconstructivist tools to understand developmental pathways to disorders
    Fischer, Kurt W.
    Connell, Michael W.
    DEVELOPMENTAL SCIENCE, 2000, 3 (01) : 24 - 26
  • [3] Diseases of development: leveraging developmental biology to understand human disease
    Dunwoodie, Sally L.
    Wallingford, John B.
    DEVELOPMENT, 2020, 147 (21):
  • [4] Disease Modeling To Understand the Pathomechanisms of Human Genetic Kidney Disorders
    Molinari, Elisa
    Sayer, John A.
    CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2020, 15 (06): : 855 - 872
  • [5] Challenges of using animal and in vitro models to understand human developmental toxicology
    van Duursen, M.
    TOXICOLOGY LETTERS, 2022, 368 : S39 - S39
  • [6] Translating Developmental Neuroscience to Understand Risk for Psychiatric Disorders
    Meyer, Heidi C.
    Lee, Francis S.
    AMERICAN JOURNAL OF PSYCHIATRY, 2019, 176 (03): : 179 - 185
  • [7] Translating Developmental Neuroscience to Understand Risk for Psychiatric Disorders
    Meyer, Heidi C.
    Lee, Francis S.
    AMERICAN JOURNAL OF PSYCHIATRY, 2023, 180 (08): : 540 - 547
  • [8] Using mouse genetics to understand human skeletal disease
    Youlten, Scott E.
    Baldock, Paul A.
    BONE, 2019, 126 : 27 - 36
  • [9] The benefits of exploiting rare genetic disorders to better understand human health and disease
    Tee, Andrew R.
    SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2016, 52 : 1 - 2
  • [10] Seeing the future: using Xenopus to understand eye regeneration
    Tseng, Ai-Sun
    GENESIS, 2017, 55 (1-2)