analysis revealed that wild-type and aMTOC-
free mouse oocytes had a comparable fraction
of mobile mClover3-KIFC1, but the turnover
of mClover3-KIFC1 at the spindle poles was
two times slower in the absence of aMTOCs
(Fig. 8, D to F). By contrast, the absence of
aMTOCs did not affect either the turnover of
mClover3-KIFC1 in the central region of the
spindle or the turnover of the microtubule
reporter mScarlet-MAP4-MTBD (fig. S14, E
to G). Thus, the dynamics of KIFC1 at the
spindle poles is specifically altered in the
absence of aMTOCs, and KIFC1 accumula-
tion at the poles may stabilize aMTOC-free
spindles.
Soet al.,Science 375 , eabj3944 (2022) 11 February 2022 9 of 19
B
Merge
A
Control IgG
bTRIM21
Merge
Merge
anti-KIFC1-C
Microtubules
Microtubules
8:42 15:02 17:45 19:12 19:56 21:23
4:35 6:58 12:04 13:56 14:37 15:08
Microtubules
4 h:18 min 7:23 10:18 12:01 13:44 14:56
Chromosomes
Control
IgG
( 34 )
anti-
KIFC1
( 32 )
0
20
40
60
80
100
Percentage of spindles
With spindle instability
Without spindle instability
D
KIFC1-
depleted
bovine oocytes
( 26 )
Human oocytes
with multipolar
spindle
intermediates ( 47 )
0
20
40
60
80
100
Percentage of spindles
Bipolarity not restored at
anaphase onset
Bipolarity restored at
anaphase onset
Control
IgG
( 33 )
anti-
KIFC1
( 26 )
0
20
40
60
80
100
Percentage of oocytes
Misaligned chromosomes
at anaphase onset
Aligned chromosomes
at anaphase onset
E
Control
IgG
( 32 )
anti-
KIFC1
( 27 )
0
20
40
60
80
100
Percentage of oocytes
With severely lagging
chromosomes
With mildly lagging
chromosomes
No lagging chromosomes
F
Control
IgG
( 41 )
anti-
KIFC1
( 31 )
0
20
40
60
80
100
Percentage of oocytes
≥2 chromosomes gained/lost
1 chromosome gained/lost
No chromosome gained/lost
G
C
Percentage of oocytes
Cont
ro
l^ bovine
oocy
tes (
33
)
KIFC1-de
plete
d
bo
vine oocytes
(^28
)
Hum
an oocyt
es
(^83
)
Human oocytes
(fr
om
re
f.^
3 )
(^35
)
0
20
40
60
80
100 Tri-directional division
Bi-directional division
Fig. 6. Depletion of KIFC1 results in spindle instability and promotes
aneuploidy in bovine oocytes.(A) Still images from time-lapse movies of control
and KIFC1-depleted bovine oocytes. Green, microtubules (mClover3-MAP4-
MTBD); magenta, chromosomes (H2B-mScarlet). Time is given as hours:minutes
after NEBD. (B) Manual scoring of spindle instability in control and KIFC1-depleted
bovine oocytes (FisherÕs exact test,P< 0.0001). (C) Quantification of the
directionality of anaphase I in control and KIFC1-depleted bovine oocytes, and in
human oocytes from ( 2 , 3 ). (D) Quantification of spindle bipolarity restoration at
anaphase onset in KIFC1-depleted bovine oocytes and in human oocytes with
multipolar spindle intermediates from ( 2 ). (E) Quantification of chromosome
misalignment at anaphase onset in control and KIFC1-depleted bovine oocytes.
(F) Quantification of chromosome missegregation during anaphase in control and
KIFC1-depleted bovine oocytes. (G) Quantification of chromosome counts at
metaphase II in control and KIFC1-depleted bovine oocytes. Yellow dashed lines
highlight spindle poles. Yellow arrowheads highlight directions of anaphase I. The
number of oocytes analyzed is specified in italics. Scale bars are 5mm.
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