Multifaceted Microcephaly-Related Gene MCPH1

MCPH1, or BRIT1, is often mutated in human primary microcephaly type 1, a neurodevelopmental disorder characterized by a smaller brain size at birth, due to its dysfunction in regulating the proliferation and self-renewal of neuroprogenitor cells. In the last 20 years or so, genetic and cellular studies have identified MCPH1 as a multifaceted protein in various cellular functions, including DNA damage signaling and repair, the regulation of chromosome condensation, cell-cycle progression, centrosome activity and the metabolism. Yet, genetic and animal model studies have revealed an unpredicted essential function of MPCH1 in gonad development and tumorigenesis, although the underlying mechanism remains elusive. These studies have begun to shed light on the role of MPCH1 in controlling various pathobiological processes of the disorder. Here, we summarize the biological functions of MCPH1, and lessons learnt from cellular and mouse models of MCPH1.

Mouse CHD4-NURD is Required for Neonatal Spermatogonia Survival and Normal Gonad Development.

Testis development and sustained germ cell production in adults rely on the establishment and maintenance of spermatogonia stem cells and their proper differentiation into spermatocytes. Chromatin remodeling complexes regulate critical processes during gamete development by restricting or promoting accessibility of DNA repair and gene expression machineries to the chromatin. Here, we investigated the role of CHD4 and CHD3 catalytic subunits of the NURD complex during spermatogenesis. Germ cell-specific deletion of Chd4 early in gametogenesis, but not Chd3, resulted in arrested early gamete development due to failed cell survival of neonate undifferentiated spermatogonia stem cell population. Candidate assessment revealed that CHD4 controls expression of Dmrt1 and its downstream target Plzf, both described as prominent regulators of spermatogonia stem cell maintenance. Our results show the requirement of CHD4 in mammalian gametogenesis pointing to functions in gene expression early in the process.

GROWTH AND EARLY REPRODUCTION DEVELOPMENT OF THE FIRST GENERATION OF SHEATFISH, Ompok miostoma (Vaillant, 1902) REARED IN CONTROLLED CONCRETE TANKS

This study was conducted to observe the growth and reproductive biology of wild sheatfish in controlled concrete tanks. The research was carried out from January to November 2020 at the Research Station for Freshwater Fisheries Germplasm, Cijeruk, Bogor. Sampled fish were captured from Cilala Lake in Bogor and Cipanas River in Sumedang, West Java. The collected fish were 14.6 ± 2.24 cm in length and 21.5 ± 9.19 g in weight. Growth and reproductive biology parameters were measured every 30 days. Cortisol, estradiol, vitellogenin, testosterone, glucose, and hemoglobin were also determined as the supporting parameters for gonadal maturity. Measured water quality parameters were temperature, pH, dissolved oxygen, ammonia, and alkalinity. The results showed that sheatfish grew with a specific growth rate of 0.4 ± 0.15%/day, FCR of 3.2 ± 0.26, and survival rate of 100%. Observation on the gonad maturity found that the fish studied were in the level-I and II. There are no significant differences regarding the supporting parameters (P>0.05) on the fish examined, despite the tendency of decreasing cortisol, and increasing testosterone. Based on the results, this study concludes that the observed fish can adapt, grow, and start to mature their gonads in their new environment, with temperature as one of the possible key factors influencing its gonad development.

OVARY DEVELOPMENT, FSH AND LH GENES EXPRESSION OF INDONESIAN LEAFFISH, Pristolepis grootii (Bleeker, 1852), INJECTED WITH LUTEINIZING HORMONE-RELEASING HORMONE ANALOG

Indonesian leaffish, Pristolepis grootii (Bleeker, 1852), is an undomesticated freshwater fish species native to the rivers, flooded swamps, and tributaries of Indonesia. The fish is mainly captured for consumption. In order to prevent its extinction and supply its growing demands, the artificial breeding of the fish should be developed. The purpose of this study was to determine the optimum dose of luteinizing hormone-releasing hormone analog (LHRHa) for stimulating the female P. grootii gonadal development at a dosage of 0, 1, 10, and 50 µg kg-1 of fish. Female fish (20.0 ± 0.6 g) were adapted for 30 days in the rearing environment and then separated into 12 aquariums with six fish per aquarium. Fish were then reared for another 21 days and fed with Tubifex sp. The LHRHa injection was conducted twice on day-7 and 14. Fish bodyweight, gonadosomatic index, gonad histology, blood estradiol-17â, and FSH-â and LH-â gene expression were evaluated at day 0, 7, 14, and 21. The results showed that the injection of the LHRHa hormone stimulated the development of fish gonads and was better achieved with a higher concentration of LHRHa. The best treatment was observed by the administration of 50 µg kg-1 of LHRHa that produced the fastest development among all treatments. This study demonstrated that the LHRHa induction could potentially stimulate the gonadal development of the newly domesticated fish. To our knowledge, this is the first study that reported the success of the induction of female gonad development in the Indonesian leaffish P. grooti.KEYWORDS:

Modest sexual size dimorphism and allometric growth: a study based on growth and gonad development in the wolf spider Pardosa pseudoannulata (Araneae: Lycosidae)

ABSTRACT Sexual size dimorphism (SSD) is a notable phenomenon in terrestrial animals, and it is correlated with unusual morphological traits. To date, the underlying sex-specific growth strategies throughout the ontogenetic stage of spiders are poorly understood. Here, we comprehensively investigated how the growth trajectories and gonad development shaped SSD in the wolf spider Pardosa pseudoannulata (Araneae: Lycosidae). We also hypothesized the potential growth allometry among the carapace, abdomen, and gonads of spiders in both sexes. By measuring the size of the carapace and abdomen, investigating developmental duration and growth rate, describing the gonadal sections, and calculating the area of gonads at all instars from hatching to maturity, we demonstrated that SSD results from sex-specific growth strategies. Our results indicated that the growth and developmental differences between both sexes appeared at early life stages, and there was allometric growth in the carapace, abdomen, and gonads between males and females.

Single-cell transcriptome reveals insights into the development and function of the zebrafish ovary

Zebrafish are an established research organism that has made many contributions to our understanding of vertebrate tissue and organ development, yet there are still significant gaps in our understanding of the genes that regulate gonad development, sex, and reproduction. Unlike the development of many organs, such as the brain and heart that form during the first few days of development, zebrafish gonads do not begin to form until the larval stage (≥5 dpf). Thus, forward genetic screens have identified very few genes required for gonad development. In addition, bulk RNA sequencing studies which identify genes expressed in the gonads do not have the resolution necessary to define minor cell populations that may play significant roles in development and function of these organs. To overcome these limitations, we have used single-cell RNA sequencing to determine the transcriptomes of cells isolated from juvenile zebrafish ovaries. This resulted in the profiles of 10,658 germ cells and 14,431 somatic cells. Our germ cell data represents all developmental stages from germline stem cells to early meiotic oocytes. Our somatic cell data represents all known somatic cell types, including follicle cells, theca cells and interstitial stromal cells. Further analysis revealed an unexpected number of cell subpopulations within these broadly defined cell types. To further define their functional significance, we determined the location of these cell subpopulations within the ovary. Finally, for select examples, we used gene knockout experiments to determine the role of newly identified genes. Our results reveal novel insights into ovarian development and function and the sequencing information will provide a valuable resource for future studies.